Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

162442

Sigma-Aldrich

2-Chloro-4-fluorophenol

99%

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
ClC6H3(F)OH
CAS Number:
1996-41-4
Molecular Weight:
146.55
Beilstein:
1861277
EC Number:
217-876-7
MDL number:
MFCD00002168
UNSPSC Code:
12352100
PubChem Substance ID:
24849982
NACRES:
NA.22

Assay

99%

form

solid

refractive index

n20/D 1.53 (lit.)

bp

88 °C/4 mmHg (lit.)

mp

23 °C (lit.)

density

1.344 g/mL at 25 °C (lit.)

functional group

chloro
fluoro

SMILES string

Oc1ccc(F)cc1Cl

InChI

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

InChI key

IGYXYGDEYHNFFT-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

2-Chloro-4-fluorophenol was used in enzymatic production of fluorocatechols.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

167.0 °F - closed cup

Flash Point(C)

75 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
05321CJ
12002KD
U16558
01408HD
U15053

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Inna P Solyanikova et al.
Applied and environmental microbiology, 69(9), 5636-5642 (2003-09-06)
The present study describes the (19)F nuclear magnetic resonance analysis of the conversion of 3-halocatechols to lactones by purified chlorocatechol 1,2-dioxygenase (ClcA2), chloromuconate cycloisomerase (ClcB2), and chloromuconolactone dehalogenase (ClcF) from Rhodococcus opacus 1cp grown on 2-chlorophenol. The 3-halocatechol substrates were

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service