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130915

Sigma-Aldrich

2-Bromophenol

98%

Synonyme(s) :

o-Bromophenol

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About This Item

Formule linéaire :
BrC6H4OH
Numéro CAS:
95-56-7
Poids moléculaire :
173.01
Numéro Beilstein :
1905115
Numéro CE :
202-432-7
Numéro MDL:
MFCD00002146
Code UNSPSC :
12352100
ID de substance PubChem :
24847983
Nomenclature NACRES :
NA.22

Pureté

98%

Forme

liquid

Indice de réfraction

n20/D 1.589 (lit.)

Point d'ébullition

195 °C (lit.)

Pf

3-7 °C (lit.)

Densité

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

Chaîne SMILES 

Oc1ccccc1Br

InChI

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

Clé InChI

VADKRMSMGWJZCF-UHFFFAOYSA-N

Informations sur le gène

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.

Pictogrammes

FlameExclamation markEnvironment
GHS02,GHS07,GHS09

Mention d'avertissement

Warning

Classification des risques

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

Organes cibles

Respiratory system

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

107.6 °F - closed cup

Point d'éclair (°C)

42 °C - closed cup

Équipement de protection individuelle

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
Catherine S Evans et al.
Environmental science & technology, 37(24), 5574-5580 (2004-01-14)
Brominated hydrocarbons are the most commonly used flame retardants. Materials containing brominated hydrocarbons are frequently disposed in municipal and hazardous waste incinerators as well as being subjected to thermal reaction in accidental fires. This results in the potential for formation
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
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
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