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Assay
95%
form
solid
mp
40-42 °C (lit.)
functional group
fluoro
SMILES string
Oc1cc(F)ccc1F
InChI
1S/C6H4F2O/c7-4-1-2-5(8)6(9)3-4/h1-3,9H
InChI key
INXKVYFOWNAVMU-UHFFFAOYSA-N
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General description
Conversion of 2,5-difluorophenol by whole cells of Rhodococcus opacus 1G has been investigated by 9F NMR analysis.
Application
2,5-Difluorophenol has been used in the synthesis of di- or trifluorinated hydroxybenzoic acids.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Sol. 1 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
4.1B - Flammable solid hazardous materials
WGK
WGK 3
Flash Point(F)
127.4 °F - closed cup
Flash Point(C)
53 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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The regioexhaustive functionalization of difluorophenols and trifluorophenols through organometallic intermediates.
Synthesis, 2004(10), 1609-1618 (2004)
FEMS microbiology letters, 181(1), 73-82 (1999-11-24)
The regiospecificity of hydroxylation of C2-halogenated phenols by Rhodococcus opacus 1G was investigated. Oxidative defluorination at the C2 position ortho with respect to the hydroxyl moiety was preferred over hydroxylation at the non-fluorinated C6 position for all 2-fluorophenol compounds studied.
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