585-76-2 Archives - Page 12 of 14 - Bromides-buliding-blocks

Gavara, Laurent team published research in Bioorganic Chemistry 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. , Formula: C7H5BrO2

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. Formula: C7H5BrO2.

Gavara, Laurent;Legru, Alice;Verdirosa, Federica;Sevaille, Laurent;Nauton, Lionel;Corsica, Giuseppina;Mercuri, Paola Sandra;Sannio, Filomena;Feller, Georges;Coulon, Remi;De Luca, Filomena;Cerboni, Giulia;Tanfoni, Silvia;Chelini, Giulia;Galleni, Moreno;Docquier, Jean-Denis;Hernandez, Jean-Francois research published 《 4-Alkyl-1,2,4-triazole-3-thione analogues as metallo-β-lactamase inhibitors》, the research content is summarized as follows. In Gram-neg. bacteria, the major mechanism of resistance to β-lactam antibiotics is the production of one or several β-lactamases (BLs), including the highly worrying carbapenemases. Whereas inhibitors of these enzymes were recently marketed, they only target serine-carbapenemases (e.g. KPC-type), and no clin. useful inhibitor is available yet to neutralize the class of metallo-β-lactamases (MBLs). We are developing compounds based on the 1,2,4-triazole-3-thione scaffold, which binds to the di-zinc catalytic site of MBLs in an original fashion, and we previously reported its promising potential to yield broad-spectrum inhibitors. However, up to now only moderate antibiotic potentiation could be observed in microbiol. assays and further exploration was needed to improve outer membrane penetration. Here, we synthesized and characterized a series of compounds possessing a diversely functionalized alkyl chain at the 4-position of the heterocycle. We found that the presence of a carboxylic group at the extremity of an alkyl chain yielded potent inhibitors of VIM-type enzymes with Ki values in the μM to sub-μM range, and that this alkyl chain had to be longer or equal to a Pr chain. This result confirmed the importance of a carboxylic function on the 4-substituent of 1,2,4-triazole-3-thione heterocycle. As observed in previous series, active compounds also preferentially contained Ph, 2-hydroxy-5-methoxyphenyl, naphth-2-yl or m-biphenyl at position 5. However, none efficiently inhibited NDM-1 or IMP-1. Microbiol. study on VIM-2-producing E. coli strains and on VIM-1/VIM-4-producing multidrug-resistant K. pneumoniae clin. isolates gave promising results, suggesting that the 1,2,4-triazole-3-thione scaffold worth continuing exploration to further improve penetration. Finally, docking experiments were performed to study the binding mode of alkanoic analogs in the active site of VIM-2.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Fu, Yatong team published research in Inorganic Chemistry in 2022 | 585-76-2

Quality Control 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.

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, Quality Control of 585-76-2

Fu, Yatong;Li, Yu;Luo, Donghong;Lu, Yibo;Huang, Jiajun;Yang, Ziyi;Lu, Jian;Jiang, Yuan-Ye;Lu, Ju-You research published 《 Palladium-Catalyzed Regioselective B(3,4)-H Acyloxylation of o-Carboranes》, the research content is summarized as follows. The authors disclosed herein an efficient regioselective B(3,4)-H activation via a ligand strategy, affording B(3)-monoacyloxylated and B(3,4)-diacyloxylated o-carboranes. The identification of amino acid and H₃PO₄ ligand was crucial for the success of B(3)-mono- and B(3,4)-diacyloxylation, resp. This ligand approach was compatible with a broad range of carboxylic acids. The functionalization of complex drug mols. was demonstrated. Other acyloxyl sources, including NaOBz, benzoic anhydride and iodobenzene diacetate, were also tolerated.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Fang, Ze-Yu team published research in Chemistry & Biodiversity in 2022 | 585-76-2

Fang, Ze-Yu;Zhang, Yi-Heng;Chen, Chong-Hao;Zheng, Qi;Lv, Peng-Cheng;Ni, Lei-Qiang;Sun, Juan;Wu, Yuan-Feng research published 《 Design, Synthesis and Molecular Docking of Novel Quinazolinone Hydrazide Derivatives as EGFR Inhibitors》, the research content is summarized as follows. A series of novel quinazolinone hydrazide derivatives were designed and synthesized as EGFR inhibitors. The results indicated that most of the aimed compounds had potential anti-tumor cell proliferation and EGFR inhibitory activities. In the comprehensive anal. of all the tested compounds, the target compound 9c showed the best anti-tumor cell proliferation activity, (IC50=1.31 μM for MCF-7, IC50=1.89 μM for HepG2, IC50=2.10 μM for SGC), and IC50=0.59 μM for the EGFR inhibitory activity. Docking results showed that compound 9c could ideally insert the active site and interact with the critical amino acid residues (Val702, Lys721, Met769, Asp831) in the active site.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Empel, Claire team published research in Organic Letters in 2021 | 585-76-2

Safety of 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.

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. Safety of 3-Bromobenzoic acid.

Empel, Claire;Nguyen, Thanh Vinh;Koenigs, Rene M. research published 《 Tropylium-Catalyzed O-H Insertion Reactions of Diazoalkanes with Carboxylic Acids》, the research content is summarized as follows. Herein, the application of a nonbenzenoid aromatic carbocation, namely tropylium, as an organic Lewis acid catalyst in O-H functionalization reactions of diazoalkanes with benzoic acids is described. The newly developed protocol is applicable to a wide range of diazoalkane and carboxylic acid substrates with excellent efficiency (43 examples, up to 99% yield).

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Dikusar, E. A. team published research in Russian Journal of General Chemistry in 2022 | 585-76-2

Dikusar, E. A.;Akishina, E. A.;Petkevich, S. K.;Zhukouskaya, N. A.;Alekseyev, R. S.;Bumagin, N. A.;Shahab, S. N.;Filippovich, L. N.;Potkin, V. I. research published 《 Synthesis of Bisacridine Derivatives with Pyridine and 1,2-Azole Fragments》, the research content is summarized as follows. The authors developed a convenient one-step method for the synthesis of new bisacridine derivatives, containing 5-arylisoxazoles, 4,5-dichloroisothiazole, as well as isonicotinic acid residues covalently attached by ester groups to various positions of the aromatic core. A three-component cascade condensation of 1,5-naphthalenediamine, aldehydes, and cyclic β-dicarbonyl compounds was carried out by refluxing in butanol. Quaternary ammonium salts of the synthesized bisacridine derivatives were obtained. Tthe synthesized bisacridine compounds form complexes with palladium LPdCl₂, which exhibit high catalytic activity in a model Suzuki reaction in water in the absence of organic co-solvent.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Dong, Chaomin team published research in Angewandte Chemie, International Edition in 2021 | 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.

Dong, Chaomin;Wang, Xiao;Gong, Wenqi;Ma, Wenbo;Zhang, Meng;Li, Jingjie;Zhang, Yuan;Zhou, Zixing;Yang, Zhijian;Qu, Shuli;Wang, Qian;Zhao, Zhu;Yang, Guohui;Lv, Anqi;Ma, Huili;Chen, Qiushui;Shi, Huifang;Yang, Yang;An, Zhongfu research published 《 Influence of Isomerism on Radioluminescence of Purely Organic Phosphorescence Scintillators》, the research content is summarized as follows. There are few reports about purely organic phosphorescence scintillators, and the relation between mol. structures and radioluminescence in organic scintillators is still unclear. An isomerism strategy to study the effect of mol. structures on radioluminescence is presented. Bromobenzoic acid (BA) isomers can achieve phosphorescence efficiency of ≤22.8% by UV irradiation Under x-ray irradiation, both m-BA and p-BA show excellent radioluminescence, while o-BA has almost no radioluminescence. Through exptl. and theor. study, radioluminescence was not only affected by nonradiation in emissive process, but also highly depended on the material conductivity caused by the different mol. packing. This study allows clear understanding of the relation between the mol. structures and radioluminescence and provides a guidance to rationally design new organic scintillators.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Cordone, Pierpaolo team published research on Bioorganic & Medicinal Chemistry Letters in 2021 | 585-76-2

Cordone, Pierpaolo;Namballa, Hari K.;Muniz, Bryant;Pal, Rajat K.;Gallicchio, Emilio;Harding, Wayne W. research published 《 New tetrahydroisoquinoline-based D₃R ligands with an o-xylenyl linker motif》, the research content is summarized as follows. The effect of rigidification of the Bu linker region of tetrahydroisoquinoline-containing D3R ligands via inclusion of an o-xylenyl motif was examined in this study. Generally, rigidification with an o-xylenyl linker group reduces D3R affinity and neg. impacts selectivity vs. D2R for compounds possessing a 6-methoxy-1,2,3,4,-tetrahydroisoquinolin-7-ol primary pharmacophore group. However, D3R affinity appears to be regulated by the primary pharmacophore group and high affinity D3R ligands with 6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline and 6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline primary pharmacophore groups were identified. The results of this study also indicate that D3R selectivity vs. the σ2R is dictated by the benzamide secondary pharmacophore group, this being facilitated with 4-substituted benzamides. Compounds 5s and 5t were identified as high affinity (Ki < 4 nM) D3R ligands. Docking studies revealed that the added Ph ring moiety interacts with the Cys181 in D3R which partially accounts for the strong D3R affinity of the ligands.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Dai, Rongke team published research on Journal of Molecular Structure in 2022 | 585-76-2

Dai, Rongke;Li, Tao;Xiao, Shengnan;Chen, Yu;Gao, Jiaming;Su, Guangyue;Zhao, Yuqing research published 《 Synthesis of panaxadiol thiadiazole derivatives and study on its potential cell cycle arrest》, the research content is summarized as follows. In this study, panaxadiol (PD) derivs, I [R¹ = 2-Me, 3-O₂N, 3,4,5-trimethoxy, etc.] and II [R² = H, AcO] were designed and synthesized by the reaction of thiadiazoles with PD. The identity of all final products I and II was elucidated by ¹H, ¹³C NMR, HR-MS. The cytotoxicity activities of the derivatives I and II were evaluated against four cancer cell lines using the MTT assay which revealed they indicated excellent anticancer activity. Among these compounds, II [R² = H] had the most significant cytotoxicity and distinctly inhibited the growth of a variety of tumor cells. Further studies showed that compound II [R² = H] could decrease the expression levels of CDKs protein family and Cyclin D1 in A549, suggesting that compound II [R² = H] could block the cell cycle. To prove the above conclusions, the binding sites of the two proteins were simulated by mol. docking method. The results demonstrated that the docking scores of II [R² = H] and the two cyclins are higher than that of PD. Based on the complex of the target protein and ligand, it was speculated that the enhanced antiproliferative activity may be related to the increased hydrogen bonding interactions. Therefore, these data provide a reference that compound II [R² = H] could be a promising lead drug for cancer treatment.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Choi, Isaac team published research on Angewandte Chemie, International Edition in 2021 | 585-76-2

Reference 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.

Organobromine compounds, also called organobromides, are organic compounds that contain carbon bonded to bromine. 585-76-2, formula is C7H5BrO2, The most pervasive is the naturally produced bromomethane. Reference of 585-76-2

Choi, Isaac;Messinis, Antonis M.;Hou, Xiaoyan;Ackermann, Lutz research published 《 A Strategy for Site- and Chemoselective C-H Alkenylation through Osmaelectrooxidative Catalysis》, the research content is summarized as follows. Osmaelectrocatalyzed C-H activations that set the stage for electrooxidative alkynes e.g., 1-methoxy-4-[2-(4-methoxyphenyl)ethynyl]benzene annulations by benzoic acids e.g., 2-methylbenzoic acid were described. The osmium electrocatalysis enables site- and chemoselective electrooxidative C-H activations with unique levels of selectivity. The isolation of unprecedented osmium(0) I and osmium(II) intermediates [OsCl₂(p-cymene)]₂, along with crystallog. characterization and analyses by spectrometric and spectroscopic in operando techniques delineate a synergistic osmium redox catalyst regime. Detailed mechanistic studies revealed a facile C-H cleavage, which allows for an ample substrate scope, providing provide robust and user-friendly access to annulated heterocycles II.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Chen, Meihang team published research on Phosphorus, Sulfur and Silicon and the Related Elements 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.

Chen, Meihang;Lu, Daowang;Zhang, Xun;Chen, Meiyun;Dong, Changjun;Wang, Xian;Wu, Wenneng;Zhang, Guoping;Luo, Hairong research published 《 Synthesis and biological activities of novel S-β-D-glucopyranoside derivatives of 1,2,4-triazole》, the research content is summarized as follows. In this study, 14 novel S-β-D-glucopyranosides of 1,2,4-triazole derivatives were synthesized and characterized by 1H NMR, 13C NMR, and HRMS. Then their antifungal activities against Gibberella zeae (G. zeae), Botryosphaeria dothidea (B. dothidea), Phompsis sp., Phytophthora infestans (P. infestans), Thanatephorus cucumeris (T. cucumeris) and antibacterial activities against Xanthomonas oryzae pv. oryzae (Xoo), Xanthomonas citri subsp. citri (Xcc) were evaluated. Bioassay results indicated that most of the title compounds exhibited good antifungal activities. Among them, compounds , , , and showed better antifungal activities against P. infestans with EC50 values of 4.98, 4.09, 3.85, and 4.90μg/mL, resp. compared with Dimethomorph (6.06μg/mL).

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary