Category: 629-04-9

A variety of minor organobromine compounds are found in nature, but none are biosynthesized or required by mammals. 629-04-9, formula is C7H15Br, Name is 1-Bromoheptane. Organobromine compounds have fallen under increased scrutiny for their environmental impact., Related Products of 629-04-9.

Tang, Min-Min;Kanagaraj, Kuppusamy;Rebek, Julius Jr.;Yu, Yang research published 《 Role of Rim Functions in Recognition and Selectivity of Small-Molecule Guests in Water-Soluble Cavitand Hosts》, the research content is summarized as follows. Groups on the upper rim of cavitands can play major roles in the recognition of small mols. Water-soluble deep cavitands 1, 2 or 3 bearing the walls upper rim of imidazole, urea, and Me urea, resp., were synthesized and characterized as hosts of small-mol. guests. The vase forms of 1 or 2 are stabilized through H-bonding to solvent water mols. between adjacent walls. Various small alkyl organic mols. – alcs., halides, cycloalkane derivatives and heterocycles – are efficiently bound in 1. For n-alcs. (C5 to C12), the -OH end is fixed at the upper rim and the alkyl parts are in the hydrophobic cavity. The longer alc. guests (C7-C12) show coiling. Cycloalkane guests rotate rapidly on all 3 axes within the host cavity, while heterocycles show orientations placing their heteroatoms near the cavitand rim. Competition studies between alkyl chlorides, bromides and iodides showed preference for binding of iodides in 1. Competition between cavitands for hexyl halide guests halide showed the order 2>1>3.

Related Products of 629-04-9, 1-Bromoheptane is a useful research compound. Its molecular formula is C7H15Br and its molecular weight is 179.1 g/mol. The purity is usually 95%.
1-Bromoheptane is a reagent that is used for the preparation of alkylthiophienylzinc chloride.
1-Bromoheptane is a reactive compound that is used in the preparation of p-hydroxybenzoic acid, which is an intermediate in the synthesis of many natural compounds. 1-Bromoheptane has been shown to have biological properties and to inhibit mitochondrial membrane potential. It also causes cell lysis and hepatic steatosis in mice. This compound has been shown to inhibit the activity of enzymes such as acetylcholinesterase, butyrylcholinesterase, and carboxylesterase. 1-Bromoheptane can be used as a model for studying the effects on congestive heart failure by increasing cardiac workloads or decreasing myocardial contractility., 629-04-9.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organic bromides such as alkyl bromides are used as fumigants in agriculture to control insects. 629-04-9, formula is C7H15Br, Name is 1-Bromoheptane. Ethylene bromide is one of the commercially important organic bromides which are the component of leaded gasoline. HPLC of Formula: 629-04-9.

Teoh, Wei-Jing;Tun Nur Iskandar, Nur Amanina Juniasari;Yeap, Guan-Yeow;Kaneko, Kazuyoshi;Shimizu, Akio;Ito, Masato M. research published 《 Experimental and computational studies of laterally ethoxy Schiff base-ester liquid crystalline magnets》, the research content is summarized as follows. A series of liquid crystals 4-X-(3′-ethoxy-4′-alkyoxyphenyimino)anilines I (X = Me, MeO, Cl; n = 7, 8) with elongated mol. axis through the introduction of alkoxy chains containing different substituents was synthesized. The thermal-optical behaviors of these organic magnets were characterized by differential scanning calorimetry and polarized optical microscopy. Elemental anal., FT-IR and ¹H-NMR were employed to elucidate the mol. structures of the target compounds Exptl. data show that the nematic phase temperature range increases in the order of CH₃ < Cl < OCH₃. The laterally ethoxy Schiff base-ester liquid crystal with the most electroneg. Cl atom is presumed to outweigh both analogs containing CH₃ and OCH₃, leading to the highest clearing temperature (Tc) value, but the present work proved that the presence of the O atom from OCH₃ is inclined to orientate in a parallel arrangement that increases the length-to-breadth ratio and the polarizability of the mol. Computational studies on the different substituents against its kinetic stability were carried out based on the variation in the energy value of HOMO-LUMO gap (ΔE_gap). A relationship between the energy gap and the substituents under the present study shows that when the ΔE_gap increases from OCH₃ < Cl < CH₃, the chem. reactivity decreases, leading to the lowering of the clearing temperature

HPLC of Formula: 629-04-9, 1-Bromoheptane is a useful research compound. Its molecular formula is C7H15Br and its molecular weight is 179.1 g/mol. The purity is usually 95%.
1-Bromoheptane is a reagent that is used for the preparation of alkylthiophienylzinc chloride.
1-Bromoheptane is a reactive compound that is used in the preparation of p-hydroxybenzoic acid, which is an intermediate in the synthesis of many natural compounds. 1-Bromoheptane has been shown to have biological properties and to inhibit mitochondrial membrane potential. It also causes cell lysis and hepatic steatosis in mice. This compound has been shown to inhibit the activity of enzymes such as acetylcholinesterase, butyrylcholinesterase, and carboxylesterase. 1-Bromoheptane can be used as a model for studying the effects on congestive heart failure by increasing cardiac workloads or decreasing myocardial contractility., 629-04-9.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organic bromides such as alkyl bromides are used as fumigants in agriculture to control insects. 629-04-9, formula is C7H15Br, Name is 1-Bromoheptane. Ethylene bromide is one of the commercially important organic bromides which are the component of leaded gasoline. Safety of 1-Bromoheptane.

Sun, Guo-Quan;Zhang, Wei;Liao, Li-Li;Li, Li;Nie, Zi-Hao;Wu, Jin-Gui;Zhang, Zhen;Yu, Da-Gang research published 《 Nickel-catalyzed electrochemical carboxylation of unactivated aryl and alkyl halides with CO₂》, the research content is summarized as follows. A general and practical electro-reductive Ni-catalytic system, realizing the electrocatalytic carboxylation of unactivated aryl chlorides and alkyl bromides with CO₂ were reported. A variety of unactivated aryl bromides, iodides and sulfonates can also undergo such a reaction smoothly. Notably, realized the catalytic electrochem. carboxylation of aryl (pseudo)halides with CO₂ avoiding the use of sacrificial electrodes. Moreover, this sustainable and economic strategy with electron as the clean reductant features mild conditions, inexpensive catalyst, safe and cheap electrodes, good functional group tolerance and broad substrate scope. Mechanistic investigations indicated that the reaction might proceed via oxidative addition of aryl halides to Ni(0) complex, the reduction of aryl-Ni(II) adduct to the Ni(I) species and following carboxylation with CO₂.

Safety of 1-Bromoheptane, 1-Bromoheptane is a useful research compound. Its molecular formula is C7H15Br and its molecular weight is 179.1 g/mol. The purity is usually 95%.
1-Bromoheptane is a reagent that is used for the preparation of alkylthiophienylzinc chloride.
1-Bromoheptane is a reactive compound that is used in the preparation of p-hydroxybenzoic acid, which is an intermediate in the synthesis of many natural compounds. 1-Bromoheptane has been shown to have biological properties and to inhibit mitochondrial membrane potential. It also causes cell lysis and hepatic steatosis in mice. This compound has been shown to inhibit the activity of enzymes such as acetylcholinesterase, butyrylcholinesterase, and carboxylesterase. 1-Bromoheptane can be used as a model for studying the effects on congestive heart failure by increasing cardiac workloads or decreasing myocardial contractility., 629-04-9.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

One prominent application of synthetic organobromine compounds is the use of polybrominated diphenyl ethers as fire-retardants, and in fact fire-retardant manufacture is currently the major industrial use of the element bromine. 629-04-9, formula is C7H15Br, Name is 1-Bromoheptane, Quality Control of 629-04-9

Sydam, Rambabu;Ojha, Manoranjan;Deepa, Melepurath research published 《 Ionic additive in an ionogel for a large area long lived high contrast electrochromic device》, the research content is summarized as follows. Heptyl viologen (HV) based electrochromic devices (ECD) suffer from poor write-erase efficiencies and become permanently colored after a few redox switches, thus limiting their use as electrochromic windows or mirrors. This formidable issue is addressed by incorporating an ionic additive: a disodium salt of ethylenediamine tetra-acetic acid (EDTA), in the ionogel electrolyte. EDTA, via electrostatic interactions, binds to the HV+bul radical cation and prevents its’ further reduction to the undesirable pale colored neutral HV0, by wedging in-between the moieties and inhibiting their undesirable stacking. A large area HV/EDTA in gel/Prussian blue (PB) ECDs of ∼8 cm x 6 cm dimensions outperforms the HV/gel/PB ECD which is evidenced in the enhanced transmission modulation (ΔTmax: 73.1% at 606 nm), coloration efficiency (η: 346.2 cm2 C-1) and superior chromaticity coordinates (colored: L*,a,b: 40, 10, -65) compared to lower magnitudes of 69.2%, 270.3 cm2 C-1 and (L*,a,b: 50.3, 8, -48.5) resp. When evaluated as a mirror, HV/EDTA in gel/PB ECD shows a reflectance modulation of ∼65% which does not alter significantly, even at -10°C or at +60°C, ratifying its thermal robustness. The HV/EDTA in gel/PB ECD shows color and bleach times of 16 and 35 s, retains ∼93% of its’ initial contrast after 104 cycles and after aging for 2 years, continues to deliver a transmission modulation of 68%. This study successfully demonstrates a cost effective, easily implementable, scaled-up HV/EDTA in gel/PB based long-lived durable ECD for energy efficient smart window and rearview mirror applications.

629-04-9, 1-Bromoheptane is a useful research compound. Its molecular formula is C7H15Br and its molecular weight is 179.1 g/mol. The purity is usually 95%.
1-Bromoheptane is a reagent that is used for the preparation of alkylthiophienylzinc chloride.
1-Bromoheptane is a reactive compound that is used in the preparation of p-hydroxybenzoic acid, which is an intermediate in the synthesis of many natural compounds. 1-Bromoheptane has been shown to have biological properties and to inhibit mitochondrial membrane potential. It also causes cell lysis and hepatic steatosis in mice. This compound has been shown to inhibit the activity of enzymes such as acetylcholinesterase, butyrylcholinesterase, and carboxylesterase. 1-Bromoheptane can be used as a model for studying the effects on congestive heart failure by increasing cardiac workloads or decreasing myocardial contractility., Quality Control of 629-04-9

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organobromine compounds, also called organobromides, are organic compounds that contain carbon bonded to bromine. 629-04-9, formula is C7H15Br, The most pervasive is the naturally produced bromomethane. Synthetic Route of 629-04-9

Song, Zongren;Liu, Xueke;Zhang, Hao;Fang, Dawei;Ma, Xiaoxue research published 《 Investigation of physicochemical properties for novel perrhenate ionic liquid and its catalytic application towards epoxidation of olefins》, the research content is summarized as follows. A novel ionic liquid (IL) based on catalytic functional metal rhenium, [Smim][ReO₄] (1-heptyl-3-methyl-imidazolium perrhenate) was synthesized and characterized. D. and surface tension values of the IL were determined at different temperatures, and the volume and surface properties were calculated and discussed, resp. Furthermore, the synthesized ionic liquid [Smim][ReO₄] was used as a green solvent and catalyst for homogeneous catalyzed epoxidation of olefin with urea hydrogen peroxide (UHP) oxidant. The effect of factors of catalyst, oxidant, reaction time, and reaction temperature was discussed. The conversion of cyclohexene and cyclooctene is over 99% at optimum conditions. The IL [Smim][ReO₄] as catalyst and solvent are characterized by high efficiency, long service life and recoverability, which is a better green homogeneous catalyst for epoxidation of olefins.

629-04-9, 1-Bromoheptane is a useful research compound. Its molecular formula is C7H15Br and its molecular weight is 179.1 g/mol. The purity is usually 95%.
1-Bromoheptane is a reagent that is used for the preparation of alkylthiophienylzinc chloride.
1-Bromoheptane is a reactive compound that is used in the preparation of p-hydroxybenzoic acid, which is an intermediate in the synthesis of many natural compounds. 1-Bromoheptane has been shown to have biological properties and to inhibit mitochondrial membrane potential. It also causes cell lysis and hepatic steatosis in mice. This compound has been shown to inhibit the activity of enzymes such as acetylcholinesterase, butyrylcholinesterase, and carboxylesterase. 1-Bromoheptane can be used as a model for studying the effects on congestive heart failure by increasing cardiac workloads or decreasing myocardial contractility., Synthetic Route of 629-04-9

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Dehydrobromination, Grignard reactions, reductive coupling, Wittig reaction, and several nucleophilic substitution reactions are some of the principal reactions which involve organic bromides. 629-04-9, formula is C7H15Br, Name is 1-Bromoheptane. Organic compounds having carbon bonded to bromine are called organic bromides. Application of C7H15Br.

Singh, Ankita;Malhotra, Shashwat;Bimal, Devla;Bouchet, Lydia M.;Wedepohl, Stefanie;Calderon, Marcelo;Prasad, Ashok K. research published 《 Synthesis, Self-Assembly, and Biological Activities of Pyrimidine-Based Cationic Amphiphiles》, the research content is summarized as follows. Pyrimidine-based cationic amphiphiles (PCAms), i.e., di-trifluoroacetic acid salts of N1-[1′-(1”,3”-diglycinatoxy-propane-2”-yl)-1′,2′,3′-triazole-4′-yl]methyl-N3-alkylpyrimidines have been synthesized utilizing naturally occurring biocompatible precursors, like glycerol, glycine, and uracil/ thymine in good yields. Synthesized PCAms consist of a hydrophilic head group comprising TFA salt of glyceryl 1,3-diglycinate and hydrophobic tail comprising of C-7 and C-12 N3-alkylated uracil or thymine conjugated via a 4-methylene-1,2,3-triazolyl linker. The physicochem. properties of all PCAms, such as critical aggregation concentration, hydrodynamic diameter, shape, and zeta potential (surface charge) were analyzed. These PCAms were also evaluated for their anti-proliferative and anti-tubercular activities. One of the synthesized PCAm exhibited 4- to 75-fold more activity than first-line anti-tubercular drugs streptomycin and isoniazid, resp., against the multidrug resistant clin. isolate 591 of Mycobacterium tuberculosis.

Application of C7H15Br, 1-Bromoheptane is a useful research compound. Its molecular formula is C7H15Br and its molecular weight is 179.1 g/mol. The purity is usually 95%.
1-Bromoheptane is a reagent that is used for the preparation of alkylthiophienylzinc chloride.
1-Bromoheptane is a reactive compound that is used in the preparation of p-hydroxybenzoic acid, which is an intermediate in the synthesis of many natural compounds. 1-Bromoheptane has been shown to have biological properties and to inhibit mitochondrial membrane potential. It also causes cell lysis and hepatic steatosis in mice. This compound has been shown to inhibit the activity of enzymes such as acetylcholinesterase, butyrylcholinesterase, and carboxylesterase. 1-Bromoheptane can be used as a model for studying the effects on congestive heart failure by increasing cardiac workloads or decreasing myocardial contractility., 629-04-9.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organic bromides such as alkyl bromides are used as fumigants in agriculture to control insects. 629-04-9, formula is C7H15Br, Name is 1-Bromoheptane. Ethylene bromide is one of the commercially important organic bromides which are the component of leaded gasoline. Application In Synthesis of 629-04-9.

Singh, Dhandeep;Singh, Nirmal research published 《 Synthesis and Evaluation of 1-hydroxybenzotriazole Derivatives: Dual Inhibitors of Carbonic Anhydrase II and Sodium Hydrogen Exchanger I》, the research content is summarized as follows. Ischemia reperfusion injury is responsible for impaired graft functioning in organ transplants, cerebral dysfunction, ischemic heart diseases, systemic inflammatory response syndrome, gastrointestinal dysfunction, and multiple organ dysfunction syndromes. Intracellular pH is critical for cell survival in ischemia reperfusion injury. Sodium hydrogen exchanger I and carbonic anhydrase II are critical in the regulation of intracellular pH. Inhibition of sodium hydrogen exchanger I and carbonic anhydrase II during reperfusion is found to ameliorate ischemia reperfusion injury sep. An attempt is made to synthesize dual inhibitors of sodium hydrogen exchanger and carbonic anhydrase to have better potential drug mol. in ischemia reperfusion injury treatment. The hydroxybenzotriazole is considered as a central pharmacophore for this dual activity and 12 derivatives are synthesized. All derivatives are tested for sodium hydrogen exchanger I and carbonic anhydrase II inhibitory activity. The tosylate derivative is found to be the most potent derivative with IC₅₀ 158.7 +/= 8.4μM for carbonic anhydrase II and 31.07 +/= 1.06μM for sodium hydrogen exchanger I. Although the potency is less than standard drugs but this is the first report of dual inhibitor of carbonic anhydrase II and sodium hydrogen exchanger.

Application In Synthesis of 629-04-9, 1-Bromoheptane is a useful research compound. Its molecular formula is C7H15Br and its molecular weight is 179.1 g/mol. The purity is usually 95%.
1-Bromoheptane is a reagent that is used for the preparation of alkylthiophienylzinc chloride.
1-Bromoheptane is a reactive compound that is used in the preparation of p-hydroxybenzoic acid, which is an intermediate in the synthesis of many natural compounds. 1-Bromoheptane has been shown to have biological properties and to inhibit mitochondrial membrane potential. It also causes cell lysis and hepatic steatosis in mice. This compound has been shown to inhibit the activity of enzymes such as acetylcholinesterase, butyrylcholinesterase, and carboxylesterase. 1-Bromoheptane can be used as a model for studying the effects on congestive heart failure by increasing cardiac workloads or decreasing myocardial contractility., 629-04-9.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

One prominent application of synthetic organobromine compounds is the use of polybrominated diphenyl ethers as fire-retardants, and in fact fire-retardant manufacture is currently the major industrial use of the element bromine. 629-04-9, formula is C7H15Br, Name is 1-Bromoheptane, Application In Synthesis of 629-04-9

Skolia, Elpida;Gkizis, Petros L.;Nikitas, Nikolaos F.;Kokotos, Christoforos G. research published 《 Photochemical aerobic oxidation of sulfides to sulfoxides: the crucial role of wavelength irradiation》, the research content is summarized as follows. Herein, a novel, sustainable, light-driven protocol was reported for photochem. aerobic oxidation of sulfides to sulfoxides RS(O)R¹ [R = Ph, naphth-2-yl, n-Bu, etc.; R¹ = Me, Et, n-Pr, etc.], where the impact of wavelength irradiation on sulfide aerobic photooxidation was examined In this work, two different low-catalyst loading (0.05-0.5 mol%) protocols, utilizing anthraquinone as the photocatalyst (under CFL lamps or 427 nm irradiation) were developed and a catalyst-free protocol (under 370 nm irradiation) was also assessed. In addition, a broad scope of substrates was tested and extensive mechanistic studies were performed, in order to distinguish the mechanistic pathways that were followed in the different cases of aryl or alkyl sulfide oxidation under different wavelength irradiation Also implemented this protocols toward the oxidation of several intermediates en route to Sulforaphane.

629-04-9, 1-Bromoheptane is a useful research compound. Its molecular formula is C7H15Br and its molecular weight is 179.1 g/mol. The purity is usually 95%.
1-Bromoheptane is a reagent that is used for the preparation of alkylthiophienylzinc chloride.
1-Bromoheptane is a reactive compound that is used in the preparation of p-hydroxybenzoic acid, which is an intermediate in the synthesis of many natural compounds. 1-Bromoheptane has been shown to have biological properties and to inhibit mitochondrial membrane potential. It also causes cell lysis and hepatic steatosis in mice. This compound has been shown to inhibit the activity of enzymes such as acetylcholinesterase, butyrylcholinesterase, and carboxylesterase. 1-Bromoheptane can be used as a model for studying the effects on congestive heart failure by increasing cardiac workloads or decreasing myocardial contractility., Application In Synthesis of 629-04-9

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Dehydrobromination, Grignard reactions, reductive coupling, Wittig reaction, and several nucleophilic substitution reactions are some of the principal reactions which involve organic bromides. 629-04-9, formula is C7H15Br, Name is 1-Bromoheptane. Organic compounds having carbon bonded to bromine are called organic bromides. Name: 1-Bromoheptane.

Shi, Xiang;Xia, TianTian;McKamey, Brooke E.;Wu, Xian;Sun, Yue;Zhou, Weifeng;Zhang, Guangyan research published 《 Concise and Efficient Synthesis of [6]-Paradol》, the research content is summarized as follows. An efficient synthesis of [6]-paradol (I) has been performed in four steps with a 72.0% overall yield. The present method highlights com. available materials, convenient isolation with multiple crystallization without involving column chromatog., and a high-purity product (more than 99.2%), and it is amenable to large-scale synthesis.

Name: 1-Bromoheptane, 1-Bromoheptane is a useful research compound. Its molecular formula is C7H15Br and its molecular weight is 179.1 g/mol. The purity is usually 95%.
1-Bromoheptane is a reagent that is used for the preparation of alkylthiophienylzinc chloride.
1-Bromoheptane is a reactive compound that is used in the preparation of p-hydroxybenzoic acid, which is an intermediate in the synthesis of many natural compounds. 1-Bromoheptane has been shown to have biological properties and to inhibit mitochondrial membrane potential. It also causes cell lysis and hepatic steatosis in mice. This compound has been shown to inhibit the activity of enzymes such as acetylcholinesterase, butyrylcholinesterase, and carboxylesterase. 1-Bromoheptane can be used as a model for studying the effects on congestive heart failure by increasing cardiac workloads or decreasing myocardial contractility., 629-04-9.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organobromine compounds, also called organobromides, are organic compounds that contain carbon bonded to bromine. 629-04-9, formula is C7H15Br, The most pervasive is the naturally produced bromomethane. Related Products of 629-04-9

Shangguan, Zhichun;Sun, Wenjin;Zhang, Zhao-Yang;Fang, Dong;Wang, Zhihang;Wu, Si;Deng, Chao;Huang, Xianhui;He, Yixin;Wang, Ruzhu;Li, Tingxian;Moth-Poulsen, Kasper;Li, Tao research published 《 A rechargeable molecular solar thermal system below 0 °C》, the research content is summarized as follows. An optimal temperature is crucial for a broad range of applications, from chem. transformations, electronics, and human comfort, to energy production and our whole planet. Photochem. mol. thermal energy storage systems coupled with phase change behavior (MOST-PCMs) offer unique opportunities to capture energy and regulate temperature Here, we demonstrate how a series of visible-light-responsive azopyrazoles couple MOST and PCMs to provide energy capture and release below 0 °C. The system is charged by blue light at -1 °C, and discharges energy in the form of heat under green light irradiation High energy d. (0.25 MJ kg^-1) is realized through co-harvesting visible-light energy and thermal energy from the environment through phase transitions. Coatings on glass with photo-controlled transparency are prepared as a demonstration of thermal regulation. The temperature difference between the coatings and the ice cold surroundings is up to 22.7 °C during the discharging process. This study illustrates mol. design principles that pave the way for MOST-PCMs that can store natural sunlight energy and ambient heat over a wide temperature range.

Related Products of 629-04-9, 1-Bromoheptane is a useful research compound. Its molecular formula is C7H15Br and its molecular weight is 179.1 g/mol. The purity is usually 95%.
1-Bromoheptane is a reagent that is used for the preparation of alkylthiophienylzinc chloride.
1-Bromoheptane is a reactive compound that is used in the preparation of p-hydroxybenzoic acid, which is an intermediate in the synthesis of many natural compounds. 1-Bromoheptane has been shown to have biological properties and to inhibit mitochondrial membrane potential. It also causes cell lysis and hepatic steatosis in mice. This compound has been shown to inhibit the activity of enzymes such as acetylcholinesterase, butyrylcholinesterase, and carboxylesterase. 1-Bromoheptane can be used as a model for studying the effects on congestive heart failure by increasing cardiac workloads or decreasing myocardial contractility., 629-04-9.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary