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Merck

306622

Sigma-Aldrich

4-氯-3-氟苯酚

98%

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5 G
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5 G
$72.70

About This Item

线性分子式:
ClC6H3(F)OH
CAS号:
分子量:
146.55
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

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方案

98%

表单

solid

沸点

84 °C/44 mmHg (lit.)

mp

54-56 °C (lit.)

溶解性

chloroform: soluble 50 mg/mL, clear, colorless

官能团

chloro
fluoro

SMILES字符串

Oc1ccc(Cl)c(F)c1

InChI

1S/C6H4ClFO/c7-5-2-1-4(9)3-6(5)8/h1-3,9H

InChI key

XLHYAEBESNFTCA-UHFFFAOYSA-N

一般描述

4-Chloro-3-fluorophenol is hydroxylated at both ortho positions to yield different products[1].

应用

4-Chloro-3-fluorophenol was used in the synthesis of 4-chloro-3-fluoro catechol[2].

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

235.4 °F - closed cup

闪点(°C)

113 °C - closed cup

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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L Ridder et al.
European journal of biochemistry, 257(1), 92-100 (1998-11-03)
The influence of various C4/C5 substituents in catechol (1,2-dihydroxybenzene) derivatives on the overall rate of conversion by catechol-1,2-dioxygenase from Pseudomonas putida (arvilla) C1 was investigated. Using catechol, 4-methylcatechol, 4-fluorocatechol, 4-chlorocatechol, 4-bromocatechol, 4,5-difluorocatechol and 4-chloro-5-fluorocatechol, it could be demonstrated that substituents
S Peelen et al.
European journal of biochemistry, 227(1-2), 284-291 (1995-01-15)
This study describes the regioselective hydroxylation and the rates of conversion of a series of fluorinated phenol derivatives by phenol hydroxylase from the yeast Trichosporon cutaneum. The natural logarithm of the kcat value for the conversion of the phenolic substrates

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