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3-Bromobenzo[b]thiophene, 95%
3-Bromobenzo[b]thiophene, 95%
3-Bromobenzo[b]thiophene, 95%
Thermo Scientific Chemicals

3-Bromobenzo[b]thiophene, 95%

CAS: 7342-82-7 | C8H5BrS | 213.092 g/mol
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Catalog number H32948.09
also known as H32948-09
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Quantity:
10 g
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Chemical Identifiers
CAS7342-82-7
IUPAC Name3-bromo-1-benzothiophene
Molecular FormulaC8H5BrS
InChI KeySRWDQSRTOOMPMO-UHFFFAOYSA-N
SMILESBrC1=CSC2=CC=CC=C12
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SpecificationsSpecification SheetSpecification Sheet
Refractive Index1.6640-1.6700 @ 20?C
Identification (FTIR)Conforms
Appearance (Color)Clear colorless to yellow to red
FormLiquid
Assay (GC)≥94.0%
Antifungal activity of synthetic di (hetero) arylamines based on the benzo [b] thiophene moiety.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Antifungal activity of synthetic di (hetero) arylamines based on the benzo [b] thiophene moiety.

Solubility
Sparingly Soluble (0.14 g/L) (25°C).

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Richard C Larock,; Dawei Yue. Synthesis of benzo[b]thiophenes by electrophilic cyclization. Journal name. year of publication , volume issue , pg no.
  2. Eugénia Pinto,; Maria-João R.P. Queiroz,; Luís A. Vale-Silva,; João F. Oliveira,; Agathe Begouin.; Jeanne-Marie Begouin.; Gilbert Kirsch. Antifungal activity of synthetic di(hetero)arylamines based on the benzo[b]thiophene moiety . Bioorganic & Medicinal Chemistry. 2008, 16(17),8172-8177.