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Merck

130915

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24847983
EC Number:
202-432-7
Beilstein/REAXYS Number:
1905115
MDL number:
MFCD00002146
Assay:
98%
Form:
liquid

Key Documents

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InChI key

VADKRMSMGWJZCF-UHFFFAOYSA-N

InChI

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

SMILES string

Oc1ccccc1Br

assay

98%

form

liquid

Quality Level

100

Gene Information

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

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

functional group

bromo

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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.

signalword

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

3 - Flammable liquids

flash_point_f

107.6 °F - closed cup

flash_point_c

42 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
STBK6329
STBK1064
STBJ9790
STBJ7657
STBH8232

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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
Catherine S Evans et al.
Environmental science & technology, 39(7), 2128-2134 (2005-05-06)
The homogeneous, gas-phase oxidative thermal degradation of 2-bromophenol was studied in a 1 cm i.d., fused silica flow reactor at a concentration of 88 ppm, reaction time of 2.0 s, over a temperature range from 300 to 1000 degrees C.
Christian Eidamshaus et al.
Organic letters, 10(19), 4211-4214 (2008-08-30)
A one-pot synthesis of benzofurans which utilizes a palladium-catalyzed enolate arylation is described. The process demonstrates broad substrate scope and provides differentially substituted benzofurans in moderate to excellent yields. The utility of the method is further demonstrated by the synthesis
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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