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Merck

130915

Sigma-Aldrich

2-Bromophenol

98%

Sinónimos:

o-Bromophenol

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About This Item

Fórmula lineal:
BrC6H4OH
Número de CAS:
Peso molecular:
173.01
Beilstein/REAXYS Number:
1905115
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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

functional group

bromo

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

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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

wgk_germany

WGK 3

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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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
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
Anusha Jayaraman et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 910, 138-148 (2012-04-24)
This work is focused on the study of the photodegradation of 2-bromophenol under the action of UV light and sunlight. The photodegradation process has been monitored using UV-Vis spectroscopy and High Performance Liquid Chromatography coupled to diode array and mass

Protocolos

Analytical standard separation of various phenols for research and industrial applications.

Analytical standard separation of various phenols for research and industrial applications.

Analytical standard separation of various phenols for research and industrial applications.

Analytical standard separation of various phenols for research and industrial applications.

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