Category: 629-04-9

Alavi, Seyed Jamal team published research on Drug Development Research in 2021 | 629-04-9

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

Vinyl bromides undergo the Heck reaction, which involves C-C coupling with alkene to give substituted alkenes. 629-04-9, formula is C7H15Br, Name is 1-Bromoheptane. Methyl bromide is a precursor in the manufacture of several chemicals and is employed as a soil sterilant, mainly for seed production. Quality Control of 629-04-9.

Alavi, Seyed Jamal;Seyedi, Seyed Mohammad;Saberi, Satar;Safdari, Hadi;Eshghi, Hossein;Sadeghian, Hamid research published 《 Allylphenols as a new class of human 15-lipoxygenase-1 inhibitors》, the research content is summarized as follows. In this study, a series of mono- and diallylphenol derivative were designed, synthesized, and evaluated as potential human 15-lipoxygenase-1 (15-hLOX-1) inhibitors. Radical scavenging potency of the synthetic allylphenol derivatives was assessed and the results were in accordance with lipoxygenase (LOX) inhibition potency. It was found that the electronic natures of allyl moiety and para substituents play the main role in radical scavenging activity and subsequently LOX inhibition potency of the synthetic inhibitors. Among the synthetic compounds, 2,6-diallyl-4-(hexyloxy)phenol (42) and 2,6-diallyl-4-aminophenol (47) showed the best results for LOX inhibition (IC50 = 0.88 and 0.80μM, resp.).

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

Ali, Zinah Hussein team published research on Eurasian Chemical Communications in 2022 | 629-04-9

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.

Vinyl bromides undergo the Heck reaction, which involves C-C coupling with alkene to give substituted alkenes. 629-04-9, formula is C7H15Br, Name is 1-Bromoheptane. Methyl bromide is a precursor in the manufacture of several chemicals and is employed as a soil sterilant, mainly for seed production. HPLC of Formula: 629-04-9.

Ali, Zinah Hussein;Jber, Nasreen Raheem research published 《 Supramolecular discotic mesophases containing melamine-core induced by hydrogen-bonding: synthesis and characterization》, the research content is summarized as follows. The purpose of the presented research is to develop suitable hydrogen-bonding complimentary chems. to produce melamine-core supra-mol. discotic liquid crystal (LC) materials that can be employed in various applications. Authors designed and synthesized 3,5-di-(3,4′,5′-trialkoxybenzoyloxy)benzoic acid derivatives, I (R = n-hexyl, n-heptyl, and n-octyl), one of three types of long-alkyloxytailed compounds with unique hydrogen-bonding matching functional groups. The liquid crystalline characteristics were assessed using polarized optical microscopy and DSC. Smectic and nematic phases were discovered.

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

Katariya, Kanubhai D. team published research on Journal of Molecular Structure in 2022 | 629-04-9

Category: bromides-buliding-blocks, 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.

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., Category: bromides-buliding-blocks.

Nakum, Kiran J.;Katariya, Kanubhai D.;Hagar, Mohamed;Jadeja, Rajendrasinh N. research published 《 The influence of lateral hydroxyl group and molecular flexibility on the mesogenic behavior of a new homologous series based on thiophene-chalcone: Synthesis, characterization, crystal structure and DFT study》, the research content is summarized as follows. A new homologous series of rod shaped calamite liquid crystals, I [R = Et, decyl, octadecyl, etc.] based on thiophene-chalcone was prepared by condensation of 2-hydroxy-4-n-alkoxybenzaldehydes (n = 2 to 8, 10, 12, 14, 16, 18) with (E)-1-(4-aminophenyl)-3-(thiophen-2-yl)prop-2-en-1-one. FT-IR, 1H NMR, 13C NMR and mass spectroscopy were used to characterize synthesized compds I. The liquid crystal behavior of all synthetic compounds I was investigated using Differential Scanning Calorimeter (DSC) and Polarizing Optical Microscope (POM). Lower members of the homologous series, n-heptyloxy to n-dodecyloxy , were nematogenic, and higher members, n-tetradecyloxy to n-octadecyloxy , were smectogenic, whereas n-ethoxy to n-pentyloxy derivatives were non-mesogenic, and n-hexyloxy exhibited monotropic nematic phase. The n-pentyloxy derivative crystallized under monoclinic, space group P2/c with unit cell dimensions a = 16.1723(9) Å, b = 5.8603(3) Å, c = 22.4320(12) Å, β = 100.153(2) , V = 2092.69(9) Å3. The ethoxy derivative was subjected to DFT (d. functional theory) level computations and complete geometric optimization utilizing B3LYP/6-311G (d, p) basis sets and results were compared with structurally similar compound

Category: bromides-buliding-blocks, 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