3-Bromophenol, 98%
3-Bromophenol, 98%
3-Bromophenol, 98%
Thermo Scientific Chemicals

3-Bromophenol, 98%

CAS: 591-20-8 | C6H5BrO | 173.01 g/mol
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Catalog NumberQuantity
ALFA14849.0910 g
Catalog number ALFA14849.09
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Quantity:
10 g
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Specifications
Chemical Name or Material3-Bromophenol
CAS591-20-8
Health Hazard 1H302-H315-H319-H335
Health Hazard 2GHS H Statement
H302-H312-H315-H319-H335
Harmful if swallowed.
Harmful in contact with skin.
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
Health Hazard 3P261-P264b-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P362-P501c
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3-Bromophenol acts as an enzyme inhibitor. It is used in the preparation of 3-bromophenyl ester by reaction with benzoyl chloride in presence of triethylamine as a catalyst. It plays an important role as an intermediate in the manufacture of pharmaceuticals, agrochemicals and dyestuff and in organic synthesis.

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
3-Bromophenol acts as an enzyme inhibitor. It is used in the preparation of 3-bromophenyl ester by reaction with benzoyl chloride in presence of triethylamine as a catalyst. It plays an important role as an intermediate in the manufacture of pharmaceuticals, agrochemicals and dyestuff and in organic synthesis.

Solubility
Soluble in water, alkali, ethanol, ether and chloroform. Slightly soluble in carbon tetra chloride.

Notes
Light and air sensitive. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Sursvakova, V. V.; Burmakina, G. V.; Rubaylo, A. I. Optimization of the conditions of phenol determination in natural and potable waters by HPLC with sorption preconcentration. J. Anal. Chem. 2015, 70 (1), 98-105.
  2. Schuster, C.; Julich-Gruner, K. K.; Schnitzler, H.; Hesse, R.; Jager, R.; Schmidt, A. W.; Knolker, H. Total Syntheses of Murrayamine E, I, and K. J. Org. Chem. 2015, 80 (11), 5666-5673.