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

3-Bromophenol, 98%, Thermo Scientific Chemicals

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Catalog number A14849.09
also known as A14849-09
Price (USD)/ Each
51.10
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Quantity:
10 g
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Price (USD)/ Each
51.10
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3-Bromophenol, 98%, Thermo Scientific Chemicals
Catalog numberA14849.09
Price (USD)/ Each
51.10
-
Add to cart
Chemical Identifiers
CAS591-20-8
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to yellow or brown
FormLiquid/low melting solid
Assay (GC)≥97.5%
Identification (FTIR)Conforms
Refractive Index1.5950-1.6010 @ 20?C
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.