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306622

Sigma-Aldrich

4-Chloro-3-fluorophenol

98%

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About This Item

Linear Formula:
ClC6H3(F)OH
CAS Number:
348-60-7
Molecular Weight:
146.55
MDL number:
MFCD00042583
UNSPSC Code:
12352100
PubChem Substance ID:
24858492
NACRES:
NA.22

Quality Level

100

assay

98%

form

solid

bp

84 °C/44 mmHg (lit.)

mp

54-56 °C (lit.)

solubility

chloroform: soluble 50 mg/mL, clear, colorless

SMILES string

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

Related Categories

General description

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

Application

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

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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
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

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