587-04-2
587-04-2
Chemical Structure
3-Chlorobenzaldehyde
Synonym(s): m-Chlorobenzenecarboxaldehyde
- CAS No.: 587-04-2
- Formula:C7H5ClO
- Molecular Weight:140.57
IUPAC Name: 3-chlorobenzaldehyde
InChIKey: SRWILAKSARHZPR-UHFFFAOYSA-N
SMILES: O=CC1=CC(Cl)=CC=C1
Biological Activity: 3-Chlorobenzaldehyde (m-Chlorobenzenecarboxaldehyde) is a substrate of rat liver microsomal aldehyde dehydrogenase (mALDH) and undergoes mALDH-mediated dehydrogenation to generate the corresponding carboxylic acid. 3-Chlorobenzaldehyde is a chlorine-substituted aromatic benzaldehyde organic synthesis building block and can serve as an intermediate for research related to organic synthesis[1][2][3][4].
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3-Chlorobenzaldehyde | 98.71% | 3-Chlorobenzaldehyde (m-Chlorobenzenecarboxaldehyde) is a substrate of rat liver microsomal aldehyde dehydrogenase (mALDH) and undergoes mALDH-mediated dehydrogenation to generate the corresponding carboxylic acid. 3-Chlorobenzaldehyde is a chlorine-substituted aromatic benzaldehyde organic synthesis building block and can serve as an intermediate for research related to organic synthesis. | ||||||||||||||||||||
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References
- [1]. Malhi R, et al. Synthesis, characterization and antitubercular activities of heterocyclic selenosemicarbazones. Bioorganic chemistry. 2022 Sep;126:105907.
- [2]. Uddin J, et al. Chalcones: The flavonoid derivatives synthesis, characterization, their antioxidant and in vitro/in vivo antidiabetic potentials. Heliyon. 2023 Nov 1;9(11).
- [3]. Martini R, et al. Rat hepatic microsomal aldehyde dehydrogenase. Identification of 3- and 4-substituted aromatic aldehydes as substrates of the enzyme. Chemical research in toxicology. 1996;9(1):268-76.
- [4]. Karatas H, et al. Alzheimer’s Disease Drug Design by Synthesis, Characterization, Enzyme Inhibition, In Silico, SAR Analysis and MM-GBSA Analysis of Schiff Bases Derivatives: H. Karatas et al. Korean Journal of Chemical Engineering. 2025 Jul;42(8):1793-811.
