3-Bromo-2,6-dihydroxybenzoic acid

3-Bromo-2,6-dihydroxybenzoic acid Suppliers list
Company Name: Shandong Mailifeng Biotechnology Co., Ltd.  Gold
Tel: 18032852911
Email: 2701131818@qq.com
Company Name: Hebei Yaocheng Pharmaceutical Technology Co. Ltd  Gold
Tel: 19903117580 19903117510
Email: yc-eliu@yaochengph.com
Company Name: Suzhou Baosheng Pharmaceutical Technology Co., Ltd.,  Gold
Tel: 18616776591
Email: xuchenghao@sinch.com.cn
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: 3B Pharmachem (Wuhan) International Co.,Ltd.  
Tel: 18930552037
Email: 3bsc@sina.com

3-Bromo-2,6-dihydroxybenzoic acid manufacturers

3-Bromo-2,6-dihydroxybenzoic acid Basic information
Product Name:3-Bromo-2,6-dihydroxybenzoic acid
Synonyms:3-BroMo-γ-resorcylic Acid;Benzoic acid, 3-bromo-2,6-dihydroxy-;3-Bromo-2,6-dihydrox;3-BROMO-2,6-DIHYDROXYBE;3-Bromo-2,6-dihydroxybenzoic acid
CAS:26792-49-4
MF:C7H5BrO4
MW:233.02
EINECS:
Product Categories:Aromatics Compounds;Aromatics
Mol File:Mol File
3-Bromo-2,6-dihydroxybenzoic acid Structure
3-Bromo-2,6-dihydroxybenzoic acid Chemical Properties
Melting point 198-200°C dec.
storage temp. Sealed in dry,2-8°C
solubility Methanol, Water
form Solid
color Off-White
InChIInChI=1S/C7H5BrO4/c8-3-1-2-4(9)5(6(3)10)7(11)12/h1-2,9-10H,(H,11,12)
InChIKeyGPCLJSXGFAOJQE-UHFFFAOYSA-N
SMILESC(O)(=O)C1=C(O)C=CC(Br)=C1O
Safety Information
MSDS Information
3-Bromo-2,6-dihydroxybenzoic acid Usage And Synthesis
Chemical PropertiesOff-White Solid
Synthesis
2,6-Dihydroxybenzoic acid

303-07-1

3-BROMO-2,6-DIHYDROXYBENZOIC ACID

26792-49-4

General procedure for the synthesis of 3-bromo-2,6-dihydroxybenzoic acid from 2,6-dihydroxybenzoic acid: to a solution of the compound 2,6-dihydroxybenzoic acid (298 g, 1.93 mol, 1.0 eq.) and diisopropylamine (98 g, 0.97 mol, 0.5 eq.) in methylene chloride (3.5 L) was added batchwise N-bromosuccinimide (362 g, 2.03 mol, 1.05 eq.). 2.03 mol, 1.05 eq.) and the reaction was carried out at -78 °C. The reaction mixture was slowly warmed to room temperature and stirred for 16 h. The progress of the reaction was monitored by thin layer chromatography (TLC) until the reaction was completed. Upon completion of the reaction, the reaction mixture was evaporated to dryness and the residue was stirred in 1N hydrochloric acid (2L) for 0.5 hours. The precipitate was collected by filtration to afford the target compound 3-bromo-2,6-dihydroxybenzoic acid (370 g, 83% yield) as a light yellow solid.

References[1] Patent: WO2016/149393, 2016, A1. Location in patent: Paragraph 0277
[2] Patent: WO2016/3929, 2016, A1. Location in patent: Paragraph 0336
[3] Journal of the Chemical Society, 1963, p. 497 - 506
3-Bromo-2,6-dihydroxybenzoic acid Preparation Products And Raw materials
Raw materials2,6-Dihydroxybenzoic acid-->N-Bromosuccinimide-->Hydrochloric acid-->Diisopropylamine
Tag:3-Bromo-2,6-dihydroxybenzoic acid(26792-49-4) Related Product Information
2,6-Dihydroxybenzoic acid 5-Bromo-2,4-dihydroxybenzoic acid 3-Bromo-2-hydroxybenzoic acid 3,5-Dibromosalicylic acid 5-Bromo-2,4-dihydroxybenzoic acid monohydrate 5-Bromosalicylic acid