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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

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

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

306622-1G:
306622-BULK:
306622-5G:
306622-VAR:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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