All Photos(1)
Linear Formula:
FC6H3(CH3)OH
CAS Number:
Molecular Weight:
126.13
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
98%
refractive index
n20/D 1.515 (lit.)
bp
76 °C/5 mmHg (lit.)
mp
32 °C (lit.)
density
1.134 g/mL at 25 °C (lit.)
SMILES string
Cc1cc(O)ccc1F
InChI
1S/C7H7FO/c1-5-4-6(9)2-3-7(5)8/h2-4,9H,1H3
InChI key
RVYGYYVGWSCWGY-UHFFFAOYSA-N
Application
4-Fluoro-3-methylphenol was used to detect the aromatic metabolites in methanogenic m-cresol-degrading consortium. It was also used in the preparation of 8-fluoronaphthoquinone via Friedel Crafts acylation reaction with maleic anhydride.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 3
Flash Point(F)
206.6 °F
Flash Point(C)
97 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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K L Londry et al.
Applied and environmental microbiology, 59(7), 2229-2238 (1993-07-01)
Anaerobic sewage sludge was used to enrich a methanogenic m-cresol-degrading consortium. 6-Fluoro-3-methylphenol was synthesized and added to subcultures of the consortium with m-cresol. This caused the accumulation of 4-hydroxy-2-methylbenzoic acid. In a separate experiment, the addition of 3-fluorobenzoic acid caused
Anita Mahapatra et al.
Bioorganic & medicinal chemistry, 15(24), 7638-7646 (2007-09-25)
The naphthoquinone 7-methyljuglone (5-hydroxy-7-methyl-1,4-naphthoquinone) has previously been isolated and identified as an active component of root extracts of Euclea natalensis which displays antitubercular activity. Herein, a series of synthetic and plant-derived naphthoquinone derivates of the 7-methyljuglone scaffold have been prepared
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