130915
2-Bromophenol
98%
동의어(들):
o-Bromophenol
로그인조직 및 계약 가격 보기
크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
BrC6H4OH
CAS 번호:
Molecular Weight:
173.01
Beilstein:
1905115
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
분석
98%
양식
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
작용기
bromo
SMILES string
Oc1ccccc1Br
InChI
1S/C6H5BrO/c7-5-3-1-2-4-6(5)8/h1-4,8H
InChI key
VADKRMSMGWJZCF-UHFFFAOYSA-N
유전자 정보
human  ...  ALOX12(239),   ALOX15(246)   
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관련 카테고리
애플리케이션
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.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
107.6 °F - closed cup
Flash Point (°C)
42 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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
프로토콜
Analytical standard separation of various phenols for research and industrial applications.
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