Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

337250

Sigma-Aldrich

4-Fluoro-3-methylphenol

98%

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

About This Item

Linear Formula:
FC6H3(CH3)OH
CAS Number:
452-70-0
Molecular Weight:
126.13
MDL number:
MFCD00042296
UNSPSC Code:
12352100
PubChem Substance ID:
24860468
NACRES:
NA.22

Quality Level

100

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.)

functional group

fluoro

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.

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

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

206.6 °F - closed cup

Flash Point(C)

97 °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
MKCP8943
MKCJ6196
MKBJ3300V
MKBC0089
MKBB9208

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

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

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