585-76-2 Archives - Page 9 of 14 - Bromides-buliding-blocks

Hoque, Emdadul Md team published research in Journal of the American Chemical Society in 2021 | 585-76-2

585-76-2, 3-bromobenzoic acid is a bromobenzoic acid carrying a single bromo subsituent at the 3-position.
3-Bromobenzoic acid, also known as 3-Bromobenzoic acid, is a useful research compound. Its molecular formula is C7H5BrO2 and its molecular weight is 201.02 g/mol. The purity is usually 95%.
3-bromobenzoic acid is used as a reagent in the synthesis of deoxypodophyllotoxin derivatives with insecticidal activity. Also used as a reagent in the synthesis of thiazole derivatives with antibacterial activity.
3-bromobenzoic acid is a molecule that is classified as a Group P2. It has an electronegativity of 1.3 and an acidity of 0.8, which are both in the middle range of values for this group. 3-Bromobenzoic acid is soluble in water and is soluble in ethanol, acetone, and ether. The chemical structure of 3-bromobenzoic acid can be determined by its monoclonal antibody binding sites, electrochemical impedance spectroscopy data, and Langmuir adsorption isotherm data. 3-Bromobenzoic acid reacts with hydrochloric acid to form benzoate and HCl gas. Chronic exposure to 3-bromobenzoic acid has been shown to cause glutamate dehydrogenase inhibition, leading to an accumulation of p-hydroxybenzoic acid in the body. , SDS of cas: 585-76-2

A variety of minor organobromine compounds are found in nature, but none are biosynthesized or required by mammals. 585-76-2, formula is C7H5BrO2, Name is 3-Bromobenzoic acid. Organobromine compounds have fallen under increased scrutiny for their environmental impact., SDS of cas: 585-76-2.

Hoque, Emdadul Md;Hassan, Mirja Mahamudul Md;Chattopadhyay, Buddhadeb research published ã?Remarkably Efficient Iridium Catalysts for Directed C(sp²)-H and C(sp³)-H Borylation of Diverse Classes of Substratesã? the research content is summarized as follows. Here we describe the discovery of a new class of C-H borylation catalysts and their use for regioselective C-H borylation of aromatic, heteroaromatic, and aliphatic systems. The new catalysts have Ir-C(thienyl) or Ir-C(furyl) anionic ligands instead of the diamine-type neutral chelating ligands used in the standard C-H borylation conditions. It is reported that the employment of these newly discovered catalysts show excellent reactivity and ortho-selectivity for diverse classes of aromatic substrates with high isolated yields. Moreover, the catalysts proved to be efficient for a wide number of aliphatic substrates for selective C(sp³)-H bond borylations. Heterocyclic mols. are selectively borylated using the inherently elevated reactivity of the C-H bonds. A number of late-stage C-H functionalization have been described using the same catalysts. Furthermore, we show that one of the catalysts could be used even in open air for the C(sp²)-H and C(sp³)-H borylations enabling the method more general. Preliminary mechanistic studies suggest that the active catalytic intermediate is the Ir(bis)boryl complex, and the attached ligand acts as bidentate ligand. Collectively, this study underlines the discovery of new class of C-H borylation catalysts that should find wide application in the context of C-H functionalization chem.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Hou, Shaohua team published research in European Journal of Medicinal Chemistry in 2021 | 585-76-2

Category: bromides-buliding-blocks, 3-bromobenzoic acid is a bromobenzoic acid carrying a single bromo subsituent at the 3-position.
3-Bromobenzoic acid, also known as 3-Bromobenzoic acid, is a useful research compound. Its molecular formula is C7H5BrO2 and its molecular weight is 201.02 g/mol. The purity is usually 95%.
3-bromobenzoic acid is used as a reagent in the synthesis of deoxypodophyllotoxin derivatives with insecticidal activity. Also used as a reagent in the synthesis of thiazole derivatives with antibacterial activity.
3-bromobenzoic acid is a molecule that is classified as a Group P2. It has an electronegativity of 1.3 and an acidity of 0.8, which are both in the middle range of values for this group. 3-Bromobenzoic acid is soluble in water and is soluble in ethanol, acetone, and ether. The chemical structure of 3-bromobenzoic acid can be determined by its monoclonal antibody binding sites, electrochemical impedance spectroscopy data, and Langmuir adsorption isotherm data. 3-Bromobenzoic acid reacts with hydrochloric acid to form benzoate and HCl gas. Chronic exposure to 3-bromobenzoic acid has been shown to cause glutamate dehydrogenase inhibition, leading to an accumulation of p-hydroxybenzoic acid in the body. , 585-76-2.

Organic compounds having carbon bonded to bromine are called organic bromides. 585-76-2, formula is C7H5BrO2, Name is 3-Bromobenzoic acid. Depending on the type of carbon to which the bromine is bonded, organic bromide could be alkyl, alkenyl, alkynyl, or aryl. Category: bromides-buliding-blocks.

Hou, Shaohua;Yang, Xiping;Yang, Yuejing;Tong, Yu;Chen, Quanwei;Wan, Boheng;Wei, Ran;Lu, Tao;Chen, Yadong;Hu, Qinghua research published ã?Design, synthesis and biological evaluation of 1H-indazole derivatives as novel ASK1 inhibitorsã? the research content is summarized as follows. A series of novel ASK1 inhibitors, e.g., I and II with 1H-indazole scaffold were designed, synthesized and evaluated for their ASK1 kinase activity and AP1-HEK293 cell inhibitory effect. Systematic structure-activity relationship (SAR) efforts led to the discovery of promising compound II, which showed excellent in vitro ASK1 kinase activity and potent inhibitory effects on ASK1 in AP1-HEK293 cells. In a tumor necrosis factor-Î± (TNF-Î±)-induced HT-29 intestinal epithelial cell model, compound II exhibited a significantly protective effect on cell viability comparable to that of GS-4997; moreover, compound II exhibited no obvious cytotoxicity against HT-29 cells at concentrations up to 25Î¼M. Mechanistic research demonstrated that compound II suppressed phosphorylation in the ASK1-p38/JNK signaling pathway in HT-29 cells and regulated the expression levels of apoptosis-related proteins. Altogether, these results showed that compound II may serve as a potential candidate compound for the treatment of inflammatory bowel disease (IBD).

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Hawash, Mohammed team published research in BMC Chemistry in 2021 | 585-76-2

Related Products of 585-76-2, 3-bromobenzoic acid is a bromobenzoic acid carrying a single bromo subsituent at the 3-position.
3-Bromobenzoic acid, also known as 3-Bromobenzoic acid, is a useful research compound. Its molecular formula is C7H5BrO2 and its molecular weight is 201.02 g/mol. The purity is usually 95%.
3-bromobenzoic acid is used as a reagent in the synthesis of deoxypodophyllotoxin derivatives with insecticidal activity. Also used as a reagent in the synthesis of thiazole derivatives with antibacterial activity.
3-bromobenzoic acid is a molecule that is classified as a Group P2. It has an electronegativity of 1.3 and an acidity of 0.8, which are both in the middle range of values for this group. 3-Bromobenzoic acid is soluble in water and is soluble in ethanol, acetone, and ether. The chemical structure of 3-bromobenzoic acid can be determined by its monoclonal antibody binding sites, electrochemical impedance spectroscopy data, and Langmuir adsorption isotherm data. 3-Bromobenzoic acid reacts with hydrochloric acid to form benzoate and HCl gas. Chronic exposure to 3-bromobenzoic acid has been shown to cause glutamate dehydrogenase inhibition, leading to an accumulation of p-hydroxybenzoic acid in the body. , 585-76-2.

Hawash, Mohammed;Jaradat, Nidal;Shekfeh, Suhaib;Abualhasan, Murad;Eid, Ahmad M.;Issa, Linda research published ã?Molecular docking, chemo-informatic properties, alpha-amylase, and lipase inhibition studies of benzodioxol derivativesã? the research content is summarized as follows. Currently, available therapies for diabetes could not achieve normal sugar values in a high percentage of treated patients. In this research project, a series of 17 benzodioxole derivatives were evaluated as antidiabetic agents; that belong to three different groups were evaluated against lipase and alpha-amylase (Î±-amylase) enzymes. The results showed that 14 compounds have potent inhibitory activities against Î±-amylase with IC₅₀ values below 10Î¼g/mL. Among these compounds, 4f was the most potent compound with an IC₅₀ value of 1.11Î¼g/mL compared to the anti-glycemic agent acarbose (IC₅₀ 6.47Î¼g/mL). On the contrary, these compounds showed weak or negligible activities against lipase enzyme. However, compound 6a showed the best inhibitory anti-lipase activity with IC₅₀ 44.1Î¼g/mL. Moreover, all the synthesized compounds were undergone Molinspiration calculation, and the result showed that all compounds obeyed Lipinskis rule of five. Mol. docking studies were performed to illustrate the binding interactions between the benzodioxole derivatives and Î±-amylase enzyme pocket. Related to the obtained results it was clear that the carboxylic acid, benzodioxole ring, halogen or methoxy substituted aryl are important for the anti-amylase activities. The potent inhibitory results of some of the synthesized compounds suggest that these mols. should go further in vivo evaluation. It also suggests the benzodioxole derivatives as lead compounds for developing new drug candidates.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

He, Feng team published research in Bioorganic Chemistry in 2021 | 585-76-2

Recommanded Product: 3-Bromobenzoic acid, 3-bromobenzoic acid is a bromobenzoic acid carrying a single bromo subsituent at the 3-position.
3-Bromobenzoic acid, also known as 3-Bromobenzoic acid, is a useful research compound. Its molecular formula is C7H5BrO2 and its molecular weight is 201.02 g/mol. The purity is usually 95%.
3-bromobenzoic acid is used as a reagent in the synthesis of deoxypodophyllotoxin derivatives with insecticidal activity. Also used as a reagent in the synthesis of thiazole derivatives with antibacterial activity.
3-bromobenzoic acid is a molecule that is classified as a Group P2. It has an electronegativity of 1.3 and an acidity of 0.8, which are both in the middle range of values for this group. 3-Bromobenzoic acid is soluble in water and is soluble in ethanol, acetone, and ether. The chemical structure of 3-bromobenzoic acid can be determined by its monoclonal antibody binding sites, electrochemical impedance spectroscopy data, and Langmuir adsorption isotherm data. 3-Bromobenzoic acid reacts with hydrochloric acid to form benzoate and HCl gas. Chronic exposure to 3-bromobenzoic acid has been shown to cause glutamate dehydrogenase inhibition, leading to an accumulation of p-hydroxybenzoic acid in the body. , 585-76-2.

Vinyl bromides undergo the Heck reaction, which involves C-C coupling with alkene to give substituted alkenes. 585-76-2, formula is C7H5BrO2, Name is 3-Bromobenzoic acid. Methyl bromide is a precursor in the manufacture of several chemicals and is employed as a soil sterilant, mainly for seed production. Recommanded Product: 3-Bromobenzoic acid.

He, Feng;Wei, Panpan;Yu, Gang;Guo, Shengxin;Zheng, Zhiguo;Chen, Shunhong;Dai, Ali;Zhang, Renfeng;Wu, Zengxue;Wu, Jian research published ã?Synthesis of trans- methyl ferulate bearing an oxadiazole ether as potential activators for controlling plant virusã? the research content is summarized as follows. A series of new ferulic acid derivatives bearing an oxadiazole ether was synthesized by introducing a structure of oxadiazole into trans-ferulic acid via an ether linkage. The synthesized target compounds were evaluated in vivo for their anti-TMV (tobacco mosaic virus) activity, which indicated that some synthesized compounds displayed strong activity for controlling TMV. For protective activity, compounds 6f and 6h had the most activities of 65% and 69.8% at 500 mg L-1, resp. Compounds 6a, 6b, 6e, 6f and 6h showed > 60% curative activities at 500 mg L-1. Preliminary proteomics anal. showed that compound 6h could regulate the phenylpropanoid biosynthesis pathway and chloroplast function. These results indicated that synthesized novel ferulic acid derivatives could be used for controlling TMV.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Gurram, Swarupa Rani team published research in Chemical Papers in 2021 | 585-76-2

Gurram, Swarupa Rani;Azam, Mohammed Afzal research published ã?Design, synthesis and biological evaluation of some novel N’-(1,3-benzothiazol-2-yl)-arylamide derivatives as antibacterial agentsã? the research content is summarized as follows. Hydroxybenzotriazole (HOBT) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDCl)-mediated synthesis of new N’-(1,3-benzothiazol-2-yl)-arylamides, I [R = 2-thienyl, 2-fluorophenyl, 4-oxochroman-3-yl, etc.] was carried out in high yields under relatively milder reaction conditions using DMF as solvent. Synthesized compounds I were characterized by FTIR, ¹H-NMR, ¹³C-NMR and HRMS spectral data. The MIC values of synthesized compounds I were determined by the broth microdilution method using Mueller Hinton medium. Tested compounds I showed variable activity against the tested Gram-pos. and Gram-neg. bacterial strains. Compounds I [R = 2,6-dichlorophenyl, 4-chloro-3-nitrophenyl; R = 3-bromophenyl, 2-iodophenyl; R = 2-thienyl, 2-quinolyl, 1H-indol-2-ylmethyl] exhibited promising activity against Staphylococcus aureus NCIM 5021 with MIC values in the range of 19.7-24.2Î¼M. Among all tested compounds, I [R = 2-thienyl] possessing thiophene ring attached to the benzothiazole moiety via amide linkage exhibited maximum activity against S. aureus NCIM 5022 with MIC of 13.0Î¼M. Compound I [R = 2-thienyl] showed maximum activity against S. aureus ATCC 43300 with MIC of 15.0Î¼M and exhibited bactericidal activity against this strain in min. bactericidal concentration determination This compound also eliminated S. aureus ATCC 43300 strain after 24-h exposure indicating its bactericidal activity. ADMET calculation showed favorable pharmacokinetic profile of synthesized compounds I.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Gu, Chengyihan team published research in Chemical Communications (Cambridge, United Kingdom) in 2022 | 585-76-2

Gu, Chengyihan;Wang, Shuaishuai;Zhang, Qingran;Xie, Jin research published ã?Visible-light-mediated amidation from carboxylic acids and tertiary amines via C-N cleavageã? the research content is summarized as follows. Synthesis of tertiary amides RC(O)NR₁R₂ [R = Ph, 4-MeC₆H₄, 4-PhC₆H₄, etc.; R¹ = R² = Et, n-Pr; R¹R² = CH₂(CH₂)₃CH₂] via iridium photocatalyzed amidation of carboxylic acids and tertiary amines through C-N bond cleavage was reported. A wide scope of structurally diverse carboxylic acids participated smoothly in the reaction, providing the desired tertiary amides with moderate-to-good yields (up to 93% yield). This amidation strategy provided an alternative way to address the regioselectivity between nucleophilic functional groups, thus complementing the functional group compatibility of classical amidation protocols. Its synthetic robustness was also proved by the late-stage modification of several complex mols. and gram-scale applications.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Guo, Chunfang team published research in Journal of Organic Chemistry in 2022 | 585-76-2

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. 585-76-2, formula is C7H5BrO2, Name is 3-Bromobenzoic acid, Reference of 585-76-2

Guo, Chunfang;Han, Xuliang;Feng, Yu;Liu, Zhaolong;Li, Yueyun;Liu, Hui;Zhang, Lizhi;Dong, Yunhui;Li, Xinjin research published ã?Straightforward Synthesis of Alkyl Fluorides via Visible-Light-Induced Hydromono- and Difluoroalkylations of Alkenes with Î±-Fluoro Carboxylic Acidsã? the research content is summarized as follows. Reported the first visible-light-induced hydromono- and difluoroalkylations of alkenes with inexpensive and easily accessible Î±-fluoro carboxylic acids. This metal-free protocol exhibits mild conditions, high efficiency and excellent functional-group tolerance, provided a straightforward approach to mono- and difluoroalkylated alkanes. Moreover, the fluorine effect on the hydrofluoroalkylation reaction was discussed in detail.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Ganesan, Moorthiamma Sarathy team published research in Journal of Heterocyclic Chemistry in 2021 | 585-76-2

Ganesan, Moorthiamma Sarathy;Raja, Kamatchi Kanmani;Murugesan, Sankaranarayanan;Karankumar, Banoth;Faheem, Faheem;Thirunavukkarasu, Sappanimuthu;Shetye, Gauri;Ma, Rui;Franzblau, Scott G.;Wan, Baojie;Rajagopal, Gurusamy research published ã?Quinoline-Proline, Triazole Hybrids: Design, Synthesis, Antituberculosis, Molecular Docking, and ADMET Studiesã? the research content is summarized as follows. A series of novel quinoline-proline hybrids I (R = Ph, 4-fluorophenyl, 4-benzoylphenyl, etc.) and quinoline-proline-1,2,3-triazole hybrids II (R¹ = OH, ethyloxidanyl, phenylaminyl) were synthesized by click chem. based on mol. hybridization concept and characterized by NMR, mass spectrometry, and elemental anal. All the titled target compounds I and II were tested for antitubercular activity by MABA and LORA methods by in vitro. Interestingly, two compounds I [R = 4-nitrophenyl (III) and 4-fluorophenyl (IV)] exhibited significant activity against the tested Mycobacterium tuberculosis H37Rv strain. Further, the cytotoxicity (CC₅₀) profile of the titled compounds against the Vero cell was performed and discussed. A mol. docking study of the hit compounds III and IV was also performed to find their putative binding interaction with the active site of the target proteins. Finally, in silico ADMET properties were also predicted for all the synthesized mols. to evaluate their drug-likeness behavior.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Gao, Hui team published research in Angewandte Chemie, International Edition in 2021 | 585-76-2

Gao, Hui;Lin, Shuang;Zhang, Shuning;Chen, Weijie;Liu, Xiawen;Yang, Guang;Lerner, Richard A.;Xu, Hongtao;Zhou, Zhi;Yi, Wei research published ã?gem-Difluoromethylene Alkyne-Enabled Diverse C-H Functionalization and Application to the on-DNA Synthesis of Difluorinated Isocoumarinsã? the research content is summarized as follows. Using gem-difluoromethylene alkynes as effectors, unprecedented diverse C-H activation/[4+2] annulations of simple benzoic acids are reported. The chemodivergent reaction outcomes are well-tuned by Rh/Ir-catalyzed system; in the Rh^III catalysis, 3-alkenyl-1H-isochromen-1-one and 3,4-dialkylideneisochroman-1-one skeletons are afforded in a solvent-dependent manner (e.g., benzoic acid + I â?II (in MeOH)/III (in TFE)) under whereas difluoromethylene-substituted 1H-isochromen-1-ones (IV) are generated under the Ir^III-catalyzed system. Mechanistic studies revealed that unusually double Î²-F eliminations and fluorine effect-induced regioselective reductive elimination are independently involved to enable distinct reaction modes for divergent product formations. Besides, synthetic application in both the derivatization of obtained diene products and the on-DNA synthesis of DNA-tagged difluorinated isocoumarin have been demonstrated, which manifested great potential for synthetic utility of the developed protocols.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Gao, Min team published research in Medicinal Chemistry (Sharjah, United Arab Emirates) in 2021 | 585-76-2

Gao, Min;Lv, QiaoLi;Zhang, HouPan;Tu, GuoGang research published ã?Synthesis and 4D-QSAR Studies of Alanine Hydroxamic Acid Derivatives as Aminopeptidase N Inhibitorsã? the research content is summarized as follows. As a target for anticancer treatment, aminopeptidase N (APN) shows its overexpression on diverse malignant tumor cells and associates with cancer invasion, angiogenesis and metastasis. The objective of the study was the design, synthesis and biol. activity evaluation of alanine hydroxamic acid derivatives as APN inhibitors, and investigation of the binding mode of inhibitors in the APN active site. Alanine hydroxamic acid derivatives were synthesized and evaluated for their in vitro anti-cancer activity using CCK-8 assay. Mol. docking and 4D-QSAR studies were carried out to suggest the mechanism of biol. activity. Compared with Bestatin, compound 9b showed the best APN inhibition activity. The putative binding mode of 9b in the APN active site was also discussed. Moreover, the robust and reliable 4D-QSAR model exhibited the following statistics: R² = 0.9352, q²_LOO = 0.8484, q²_LNO =0.7920, R²_Pred = 0.8739. Newly synthesized compounds exerted acceptable anticancer activity and further investigation of the current scaffold would be beneficial.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary