306622
4-Chloro-3-fluorophenol
98%
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About This Item
Linear Formula:
ClC6H3(F)OH
CAS Number:
Molecular Weight:
146.55
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Product Name
4-Chloro-3-fluorophenol, 98%
InChI
1S/C6H4ClFO/c7-5-2-1-4(9)3-6(5)8/h1-3,9H
SMILES string
Oc1ccc(Cl)c(F)c1
InChI key
XLHYAEBESNFTCA-UHFFFAOYSA-N
assay
98%
form
solid
bp
84 °C/44 mmHg (lit.)
mp
54-56 °C (lit.)
solubility
chloroform: soluble 50 mg/mL, clear, colorless
functional group
chloro
fluoro
Quality Level
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
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
Regulatory Information
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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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