5470-96-2
Chemical Structure
Quinoline-2-carboxaldehyde
Synonym(s): 2-Quinolinecarboxaldehyde
- CAS No.: 5470-96-2
- Formula:C10H7NO
- Molecular Weight:157.17
IUPAC Name: quinoline-2-carbaldehyde
InChIKey: WPYJKGWLDJECQD-UHFFFAOYSA-N
SMILES: O=CC1=NC2=CC=CC=C2C=C1
Biological Activity: Quinoline-2-carboxaldehyde (2-Quinolinecarboxaldehyde) is a quinoline derivative that serves as a synthetic precursor for Schiff base copper complexes. Quinoline-2-carboxaldehyde is applicable to research related to the synthetic design of biomaterials or organic compounds, such as fluorescent sensors[1][2].
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Quinoline-2-carboxaldehyde | 99.99% | Quinoline-2-carboxaldehyde (2-Quinolinecarboxaldehyde) is a quinoline derivative that serves as a synthetic precursor for Schiff base copper complexes. Quinoline-2-carboxaldehyde is applicable to research related to the synthetic design of biomaterials or organic compounds, such as fluorescent sensors. | ||||||||||||||||||||
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Similarity Score 0.86
HY-W0168408-Hydroxyquinoline-2-carbaldehyde -
Similarity Score 0.84
HY-Y0075R2-Naphthaldehyde (Standard) -
Similarity Score 0.84
HY-Y0075S12-Naphthaldehyde-13C -
Similarity Score 0.83
HY-W002011RQuinoline-2-carboxylic acid (Standard) -
Similarity Score 0.83
HY-W007524R2-Aminoquinoline (Standard) -
Similarity Score 0.81
HY-W016141Methyl quinaldate -
Similarity Score 0.80
HY-D1519Naphthalene-1,2-dicarbaldehyde -
Similarity Score 0.80
HY-W015650Indole-2-carbaldehyde -
Similarity Score 0.78
HY-W0055982-Hydroxyquinoline -
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References
- [1]. Adsule S, et al. Novel Schiff base copper complexes of quinoline-2 carboxaldehyde as proteasome inhibitors in human prostate cancer cells. J Med Chem. 2006;49(24):7242-7246. [Content Brief]
- [2]. Lee HW, et al. Quinoline-2-carboxylic acid isolated from Ephedra pachyclada and its structural derivatives show inhibitory effects against α-glucosidase and α-amylase. J Korean Soc Appl Biol Chem. 2014;57:441-444.