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

2-Bromophenol, 98%, Thermo Scientific Chemicals

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Quantity:
100 g
25 g
500 g
Catalog number A14112.22
also known as A14112-22
Price (USD)/ Each
388.00
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Quantity:
100 g
Request bulk or custom format
Price (USD)/ Each
388.00
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2-Bromophenol, 98%, Thermo Scientific Chemicals
Catalog numberA14112.22
Price (USD)/ Each
388.00
-
Add to cart
Chemical Identifiers
CAS95-56-7
IUPAC Name2-bromophenol
Molecular FormulaC6H5BrO
InChI KeyVADKRMSMGWJZCF-UHFFFAOYSA-N
SMILESOC1=CC=CC=C1Br
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to yellow or pale orange
Assay (GC)≥97.5%
Identification (FTIR)Conforms
Refractive Index1.5870-1.5910 @ 20?C
FormLiquid
2-Bromophenol used as a disinfection byproduct found in chlorinated pool water. Used in the preparation of anti-benzofurobenzofuran diimides. It was also used to study the photodegradation of 2-bromophenol using UV-Vis spectroscopy and HPLC.

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
2-Bromophenol used as a disinfection byproduct found in chlorinated pool water. Used in the preparation of anti-benzofurobenzofuran diimides. It was also used to study the photodegradation of 2-bromophenol using UV-Vis spectroscopy and HPLC.

Solubility
Soluble in chloroform and ether. Slightly soluble in water.

Notes
Light sensitive. Store in dark. Store in cool, dry place in tightly closed containers.
RUO – Research Use Only

General References:

  1. Sabin-Lucian Suraru et. al. Diindole-annulated naphthalene diimides: synthesis and optical and electronic properties of syn- and anti-isomers. Journal of Organic Chemistry. 2014, 79 (1), 128-139.
  2. Jayaraman A; Mas S; Tauler R, et al. Study of the photodegradation of 2-bromophenol under UV and sunlight by spectroscopic, chromatographic and chemometric techniques. J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 2012, 910 (1), 138-48.
  3. Reacts with n-BuLi to give a dilithio derivative, which reacts with electrophiles at carbon in a useful synthesis of ortho-substituted phenols: J. Org. Chem., 49, 5267 (1984).