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, Recommanded Product: 3-Bromobenzoic acid
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).
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.
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary