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Merck
CN

31302

2-溴苯酚

analytical standard

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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
EC Number:
202-432-7
UNSPSC Code:
41116107
PubChem Substance ID:
Beilstein/REAXYS Number:
1905115
MDL number:
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grade

analytical standard

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

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.)

application(s)

environmental

format

neat

SMILES string

Oc1ccccc1Br

InChI

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

InChI key

VADKRMSMGWJZCF-UHFFFAOYSA-N

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.


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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



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Catherine S Evans et al.
Environmental science & technology, 39(13), 4857-4863 (2005-08-02)
We studied the surface-mediated pyrolytic thermal degradation of 2-bromophenol, a model brominated hydrocarbon that may form brominated dioxins in combustion and thermal processes, on silica-supported copper oxide in a 1 mm i.d., fused silica flow reactor at a constant concentration
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