130915
2-溴苯酚
98%
别名:
o-Bromophenol
登录 查看组织和合同定价。
选择尺寸
变更视图
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
Quality Segment
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
human ... ALOX12(239), ALOX15(246)
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。
Still not finding the right product?
Explore all of our products under 2-溴苯酚
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
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
实验方案
Analytical standard separation of various phenols for research and industrial applications.
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
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
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 130915-10G | 04061838728012 |
| 130915-50G | 04061838728029 |