ChemicalBook--->CAS DataBase List--->19075-59-3

19075-59-3

19075-59-3 Structure

19075-59-3 Structure
IdentificationBack Directory
[Name]

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

19075-59-3
[Synonyms]

7-Bromobenzothiophene-2-carboxylic acid
7-Bromo-1-benzothiophene-2-carboxylic acid
7-broMo-Benzo[b]thiophene-2-carboxylic acid
Benzo[b]thiophene-2-carboxylic acid, 7-bromo-
7-Bromobenzo[b]thiophene-2-carboxylic acid 98%
7-Bromobenzo[b]thiophene-2-carboxylic acid 95+%
7-Bromo-2-carboxybenzo[b]thiophene, 7-Bromo-1-benzothiophene-2-carboxylic acid
[Molecular Formula]

C9H5BrO2S
[MDL Number]

MFCD12032270
[MOL File]

19075-59-3.mol
[Molecular Weight]

257.1
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C(protect from light)
[form ]

solid
[color ]

White
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
[HazardClass ]

IRRITANT
[HS Code ]

2916399090
Spectrum DetailBack Directory
[Spectrum Detail]

Benzo[b]thiophene-2-carboxylic acid, 7-bromo-(19075-59-3)1HNMR
Hazard InformationBack Directory
[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
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