7-Bromo-benzo[b]thiophene

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Company Name: Chengdu Aofan Pharmtech Co.,Ltd  Gold
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7-Bromo-benzo[b]thiophene manufacturers

7-Bromo-benzo[b]thiophene Basic information
Product Name:7-Bromo-benzo[b]thiophene
Synonyms:7-bromo-1-benzothiophene;7-Bromobenzothiophene;Benzo[b]thiophene, 7-broMo-;Brexpiprazole Impurity 7-bromobenzo[b]thiophene;7-Bromobenzo[b]thiophene;7-Bromobenzo[b]thiophene >;7-Bromo-benzo[b]thiophene
CAS:1423-61-6
MF:C8H5BrS
MW:213.09
EINECS:
Product Categories:
Mol File:1423-61-6.mol
7-Bromo-benzo[b]thiophene Structure
7-Bromo-benzo[b]thiophene Chemical Properties
Boiling point 109°C/10mmHg(lit.)
density 1.649±0.06 g/cm3(Predicted)
refractive index 1.6600-1.6640
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form clear liquid
color Light yellow to Yellow to Orange
InChIInChI=1S/C8H5BrS/c9-7-3-1-2-6-4-5-10-8(6)7/h1-5H
InChIKeyNOICDPBEDNMHQK-UHFFFAOYSA-N
SMILESC12=C(Br)C=CC=C1C=CS2
Safety Information
Safety Statements 24/25
HazardClass IRRITANT
HS Code 29349990
MSDS Information
7-Bromo-benzo[b]thiophene Usage And Synthesis
Uses7-Bromobenzo[b]thiophene is a useful research chemical used in the preparation of di(chloro)-N-[(benzo[b]thienyl)sulfonyl]benzamide.
Synthesis
1-BROMO-2-(2,2-DIETHOXY-ETHYLSULFANYL)-BENZENE

137105-52-3

7-BROMO-BENZO[B]THIOPHENE

1423-61-6

Preparation of 7-bromobenzo[b]thiophene of Scheme I, Step B: Chlorobenzene (100 mL) and polyphosphoric acid (30.4 g, PPA) were mixed and heated to reflux. Within 20 min, 2-(2-bromophenylthio)acetaldehyde diethyl acetal (13.7 g, 44.88 mmol, Scheme I, Step A) was dissolved in chlorobenzene (20 mL) and slowly added dropwise to the refluxed mixture. The reaction mixture was kept at reflux for 4 hours and subsequently cooled. The solvent was removed by decantation and toluene (2 x 50 mL) was added to the residue, stirred thoroughly and decanted again. The toluene extract was concentrated under vacuum and the residue was dissolved in a mixture of ethyl acetate and water. The organic phase was washed with saturated sodium bicarbonate solution, dried over anhydrous sodium sulfate, filtered and concentrated to give 7-bromobenzo[b]thiophene (8.91 g, 93% yield).

References[1] Patent: US6436964, 2002, B1
[2] Patent: US6465453, 2002, B1
[3] Patent: US6353008, 2002, B1. Location in patent: Page column 26
[4] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 14, p. 3933 - 3937
[5] Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1982, p. 1489 - 1492
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