1550-35-2
Chemical Structure
2,4-Difluorobenzaldehyde
- CAS No.: 1550-35-2
- Formula:C7H4F2O
- Molecular Weight:142.10
IUPAC Name: 2,4-difluorobenzaldehyde
InChIKey: WCGPCBACLBHDCI-UHFFFAOYSA-N
SMILES: FC1=CC(F)=C(C=O)C=C1
Biological Activity: 2,4-Difluorobenzaldehyde is a fluorinated benzaldehyde derivative commonly used as an intermediate in organic synthesis. 2,4-Difluorobenzaldehyde serves as a substrate for enzymatic oxidation and undergoes the Baeyer-Villiger oxidation reaction under the catalysis of 4-hydroxyacetophenone monooxygenase. 2,4-Difluorobenzaldehyde acts as a synthetic precursor for trichalcone enzyme inhibitors. 2,4-Difluorobenzaldehyde is applicable to related research in fields such as medicine, pesticides, and liquid crystal materials[1][2].
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2,4-Difluorobenzaldehyde | 99.51% | 2,4-Difluorobenzaldehyde is a fluorinated benzaldehyde derivative commonly used as an intermediate in organic synthesis. 2,4-Difluorobenzaldehyde serves as a substrate for enzymatic oxidation and undergoes the Baeyer-Villiger oxidation reaction under the catalysis of 4-hydroxyacetophenone monooxygenase. 2,4-Difluorobenzaldehyde acts as a synthetic precursor for trichalcone enzyme inhibitors. 2,4-Difluorobenzaldehyde is applicable to related research in fields such as medicine, pesticides, and liquid crystal materials. | ||||||||||||||||||||
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Similarity Score 0.91
HY-Y0805R3,4-Difluorobenzaldehyde (Standard) -
Similarity Score 0.88
HY-I05612-Fluoro-5-bromobenzaldehyde -
Similarity Score 0.87
HY-W0073315-Fluorosalicylaldehyde -
Similarity Score 0.84
HY-W0075184-Bromo-3-fluorobenzaldehyde -
Similarity Score 0.83
HY-W0050855-Fluoro-2-methoxybenzaldehyde -
Similarity Score 0.82
HY-34512R2,4,5-Trifluorobenzaldehyde (Standard) -
Similarity Score 0.82
HY-201382-Fluoro-5-formylbenzonitrile -
Similarity Score 0.82
HY-W0154772-Chloro-6-fluorobenzaldehyde -
Similarity Score 0.81
HY-W0020682,4-Difluorobenzoic acid -
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References
- [1]. Burmaoglu S, et al. Synthesis and biological evaluation of novel tris-chalcones as potent carbonic anhydrase, acetylcholinesterase, butyrylcholinesterase and α-glycosidase inhibitors. Bioorganic chemistry. 2019 Apr;85:191-197. [Content Brief]
- [2]. Moonen M J H, et al. Enzymatic Baeyer–Villiger Oxidation of Benzaldehydes. Advanced Synthesis & Catalysis, 2005, 347(7-8): 1027-1034.
