130915
2-溴苯酚
98%
别名:
o-Bromophenol
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关于此项目
线性分子式:
BrC6H4OH
化学文摘社编号:
分子量:
173.01
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-432-7
Beilstein/REAXYS Number:
1905115
MDL number:
Assay:
98%
Form:
liquid
产品名称
2-溴苯酚, 98%
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
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
Quality Level
Gene Information
human ... ALOX12(239), ALOX15(246)
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Application
2-溴苯酚用于制备抗苯并呋喃二酰亚胺 。并利用紫外-可见光谱和 HPLC 研究了 2-溴苯酚的光降解。
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
存储类别
3 - Flammable liquids
wgk
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
法规信息
危险化学品
此项目有
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
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
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
实验方案
Analytical standard separation of various phenols for research and industrial applications.
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