528986
2-Fluoro-4-methoxybenzaldehyde
97%
Synonym(s):
2-Fluoro-p-anisaldehyde
Sign Into View Organizational & Contract Pricing
Select a Size
About This Item
Linear Formula:
FC6H3(OCH3)CHO
CAS Number:
Molecular Weight:
154.14
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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 Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Synthesis of 1, 3-Bis (hydroxy-halogenophenyl)-propane-1, 3-diamines and their Pt (II) Complexes, Syntheses of the Ligands.
Kammermeier T and Wiegrebe W.
Arch. Pharm. (Weinheim), 327, 547-561 (1994)
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)
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
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