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130915

Sigma-Aldrich

2-Bromophenol

98%

Synonym(s):

o-Bromophenol

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About This Item

Linear Formula:
BrC6H4OH
CAS Number:
95-56-7
Molecular Weight:
173.01
Beilstein:
1905115
EC Number:
202-432-7
MDL number:
MFCD00002146
UNSPSC Code:
12352100
PubChem Substance ID:
24847983
NACRES:
NA.22

Quality Level

100

Assay

98%

form

liquid

refractive index

n20/D 1.589 (lit.)

bp

195 °C (lit.)

mp

3-7 °C (lit.)

density

1.492 g/mL at 25 °C (lit.)
1.6235 g/mL at 25 °C

SMILES string

Oc1ccccc1Br

InChI

1S/C6H5BrO/c7-5-3-1-2-4-6(5)8/h1-4,8H

InChI key

VADKRMSMGWJZCF-UHFFFAOYSA-N

Gene Information

human ... ALOX12(239) , ALOX15(246)

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Application

2-Bromophenol was 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.

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

107.6 °F - closed cup

Flash Point(C)

42 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Sabin-Lucian Suraru et al.
The Journal of organic chemistry, 79(1), 128-139 (2013-11-28)
Here we report a selective method for the core-extension of naphthalene diimide (NDI) with two annulated indole rings leading to carbazolo[2,3-b]carbazole diimides (CbDIs) with exclusive syn-connectivity based on a regioselective nucleophilic substitution reaction of Br4-NDI with arylamines, followed by palladium-catalyzed
Donna E Fennell et al.
Applied and environmental microbiology, 70(2), 1169-1175 (2004-02-10)
Terminal restriction fragment length polymorphism analysis of reverse-transcribed 16S rRNA during periods of community flux was used as a tool to delineate the roles of the members of a 2-bromophenol-degrading, sulfate-reducing consortium. Starved, washed cultures were amended with 2-bromophenol plus
Hong Chang et al.
Journal of chromatography. A, 1217(4), 506-513 (2009-12-17)
A method using high performance liquid chromatography-electrospray tandem mass spectrometry (LC-ESI-MS/MS) in positive ion mode was developed for the simultaneous analysis of 30 phenolic compounds, including four estrogens, bisphenol A (BPA), 10 hydroxylated polybrominated dephenyl ethers (OH-PBDEs) and 15 bromophenols
Miho Uchida et al.
Journal of hazardous materials, 101(3), 231-238 (2003-08-26)
2-Bromophenol was reacted in aqueous sodium hydroxide at 200-250 degrees C. The decomposition rate was remarkably faster at 250 degrees C than at 225 or 200 degrees C, and the percentage debromination reached almost 100% in 1M NaOH at 250
Catherine S Evans et al.
Environmental science & technology, 40(9), 3036-3042 (2006-05-25)
The homogeneous, gas-phase oxidative thermal degradation of a 50:50 mixture of 2-bromophenol and 2-chlorophenol was studied in a 1 cm i.d., fused silica flow reactor at a concentration of 88 ppm, with a reaction time of 2.0 s, over a
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