Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

528986

Sigma-Aldrich

2-Fluoro-4-methoxybenzaldehyde

97%

Synonym(s):

2-Fluoro-p-anisaldehyde

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

About This Item

Linear Formula:
FC6H3(OCH3)CHO
CAS Number:
331-64-6
Molecular Weight:
154.14
MDL number:
MFCD00236679
UNSPSC Code:
12352100
PubChem Substance ID:
24877633
NACRES:
NA.22

assay

97%

mp

43-48 °C (lit.)

storage temp.

2-8°C

SMILES string

COc1ccc(C=O)c(F)c1

InChI

1S/C8H7FO2/c1-11-7-3-2-6(5-10)8(9)4-7/h2-5H,1H3

InChI key

UNWQNFJBBWXFBG-UHFFFAOYSA-N

General description

2-Fluoro-4-methoxybenzaldehyde is a fluorinated aromatic aldehyde. It can be prepared from 4-bromo-3-fluoroanisole.

Application

2-Fluoro-4-methoxybenzaldehyde may be used in the preparation of:
  • fluorine containing 2,4,5-trisubstituted imidazole
  • 1-(2-fluoro-4-methoxyphenyl)-2-propanone
  • 6-(2-fluoro-4-methoxyphenyl)fulvene
  • 10-(2-fluoro-4-methoxyphenyl)-6,7,9,10-tetrahydro-1Hfuro[3,4-b]pyrazolo[3,4-f]quinolin-9-one
  • polyhydroquinoline (PHQ)
  • 3-(2-fluoro-4-methoxyphenyl) acrylic acid methyl ester

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCT8763
MKCS2573
MKBZ2818V
MKBZ4152V
MKBV6616V

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

Indium trifluoride: A highly efficient catalyst for the synthesis of fluorine-containing 2, 4, 5-trisubstituted imidazoles under solvent-free conditions.
Reddy MV and Jeong YT.
Journal of Fluorine Chemistry, 142, 45-51 (2012)
Fluorinated derivatives of titanocene Y: synthesis and cytotoxicity studies.
Claffey J, et al.
European Journal of Organic Chemistry, 26, 4074-4082 (2008)
Polystyrene-Supported p-Toluenesulfonic Acid: A New, Highly Efficient, and Recyclable Catalyst for the Synthesis of Hydropyridine Derivatives under Solvent-Free Conditions.
Reddy MV and Jeong YT.
Synlett, 23(20), 2985-2991 (2012)
Synthesis, cytotoxic activity and docking studies of new 4-aza-podophyllotoxin derivatives.
Hatti I, et al.
Medicinal Chemistry Research, 24(8), 3305-3313 (2015)
Jack G Parsons et al.
Molecules (Basel, Switzerland), 9(6), 449-458 (2007-11-17)
The synthesis of (2S)-2-benzyloxymethyl-3-(2-fluoro-4-methoxyphenyl)- propionic acid, (2S)-2-benzyloxymethyl-3-(2-fluoro-4-methylphenyl)propionic acid and (2S)-2-benzyl-oxymethyl-3-(2,4-dimethylphenyl)propionic acid has been achieved by TiCl4 mediated alkylation of the corresponding (4R)-4-benzyl-3-[3-(2-fluoro-4-methoxyphenyl-, 2-fluoro-4-methylphenyl-, 2,4- dimethylphenyl-)propionyl]-2-oxazolidinones, followed by hydrolysis of the chiral auxiliary. The stereochemistry of the alkylation reaction was confirmed
View All Related Papers

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