Benzo[b]thiophene-2-carboxylic acid, 7-bromo-

Benzo[b]thiophene-2-carboxylic acid, 7-bromo- Suppliers list
Company Name: Jia Xing Isenchem Co.,Ltd  
Tel: 0573-85285100 18627885956
Email: isenchem@163.com
Company Name: Nanjing Chemlin Chemical Co., Ltd  
Tel: 025-83697070 13770331960
Email: info@chemlin.com.cn
Company Name: Nanjing Norris-Pharm Technology Co., Ltd  
Tel: 13901585132
Email: sales@norris-pharm.com
Company Name: Haoyuan Chemexpress Co., Ltd.  
Tel: 021-58950125
Email: info@chemexpress.com
Company Name: Shanghai Run-Biotech Co., Ltd.  
Tel: 021-57171705 13817537615
Email: sales@run-biotech.com
Benzo[b]thiophene-2-carboxylic acid, 7-bromo- Basic information
Product Name:Benzo[b]thiophene-2-carboxylic acid, 7-bromo-
Synonyms:Benzo[b]thiophene-2-carboxylic acid, 7-bromo-;7-Bromo-1-benzothiophene-2-carboxylic acid;7-broMo-Benzo[b]thiophene-2-carboxylic acid;7-Bromobenzo[b]thiophene-2-carboxylic acid 98%;7-Bromo-2-carboxybenzo[b]thiophene, 7-Bromo-1-benzothiophene-2-carboxylic acid;7-Bromobenzo[b]thiophene-2-carboxylic acid 95+%;7-Bromobenzothiophene-2-carboxylic acid
CAS:19075-59-3
MF:C9H5BrO2S
MW:257.1
EINECS:
Product Categories:
Mol File:19075-59-3.mol
Benzo[b]thiophene-2-carboxylic acid, 7-bromo- Structure
Benzo[b]thiophene-2-carboxylic acid, 7-bromo- Chemical Properties
storage temp. 2-8°C(protect from light)
form solid
color White
Safety Information
HazardClass IRRITANT
HS Code 2916399090
MSDS Information
Benzo[b]thiophene-2-carboxylic acid, 7-bromo- Usage And Synthesis
Synthesis
METHYL 7-BROMO-1-BENZOTHIOPHENE-2-CARBOXYLATE

550998-53-3

Benzo[b]thiophene-2-carboxylic acid, 7-bromo-

19075-59-3

General procedure for the synthesis of 7-bromobenzo[b]thiophene-2-carboxylic acid from methyl 7-bromobenzo[b]thiophene-2-carboxylate: 7-bromobenzo[b]thiophene-2-carboxylic acid methyl ester (64 mg, 0.22 mmol) was dissolved in methanol (3 mL), followed by addition of 3 N sodium hydroxide solution (240 μL, 0.72 mmol). The reaction mixture was heated to reflux for 2 hours. Upon completion of the reaction, the reaction mixture was acidified with 3 N hydrochloric acid and extracted with ethyl acetate (30 mL). The organic phases were combined, dried over anhydrous sodium sulfate (Na2SO4) and concentrated under reduced pressure. 7-Bromobenzo[b]thiophene-2-carboxylic acid (62 mg, 0.24 mmol, 100% yield) was obtained as a white solid and did not require further purification by silica gel column chromatography.

References[1] Patent: KR2015/117318, 2015, A. Location in patent: Paragraph 0181; 0192; 0193; 0194
[2] European Journal of Medicinal Chemistry, 2017, vol. 125, p. 538 - 550
[3] Patent: WO2003/104227, 2003, A1. Location in patent: Page 47, 48
[4] Patent: EP2926660, 2015, A1. Location in patent: Paragraph 0262; 0263
Benzo[b]thiophene-2-carboxylic acid, 7-bromo- Preparation Products And Raw materials
Raw materialsMethyl 7-bromo-1-benzothiophene-2-carboxylate-->2-Bromo-3-fluorobenzaldehyde-->Methyl thioglycolate-->Methanol-->Sodium hydroxide
Tag:Benzo[b]thiophene-2-carboxylic acid, 7-bromo-(19075-59-3) Related Product Information
7-Bromo-benzo[b]thiophene 7-Bromo-1-benzofuran-2-carboxylicacid 7-Bromobenzo[d]isoxazol-3-amine 7-BroMobenzo[d]oxazol-2-aMine Coumarin 7-BroMobenzo[d]isoxazole 7-BroMo-benzothiazole-2-carboxylic acid 7-Bromobenzo[b]furan 7-Bromobenzo[d]oxazole 7-bromobenzo[b]thiophene-2-carbaldehyde 7-bromobenzo[d]thiazole-2-thiol Ethyl 7-bromobenzofuran-2-carboxylate