109363-30-6

Basic information

• Product Name: 1-(3-chlorophenyl)-5-methyl-3-phenyl-1H-pyrazolo[4,3-c]quinolin-4(5H)-one
• Synonyms: 1-(3-chlorophenyl)-5-methyl-3-phenyl-1H-pyrazolo[4,3-c]quinolin-4(5H)-one
• CAS NO: 109363-30-6
• Molecular Weight: 385.853
• Mol File: 109363-30-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-(3-chlorophenyl)-5-methyl-3-phenyl-1H-pyrazolo[4,3-c]quinolin-4(5H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-chlorophenyl)-5-methyl-3-phenyl-1H-pyrazolo[4,3-c]quinolin-4(5H)-one(109363-30-6)
• EPA Substance Registry System: 1-(3-chlorophenyl)-5-methyl-3-phenyl-1H-pyrazolo[4,3-c]quinolin-4(5H)-one(109363-30-6)

Safety Data

• Hazardous Substances Data: 109363-30-6(Hazardous Substances Data)

Upstream product

• 73281-64-8 3-benzoyl-4-hydroxy-1-methylquinolin-2(1H)-one 
• 2312-23-4 m-chlorophenylhydrazine hydrochloride 
• 39228-29-0 (E)-methyl 2-nitrocinnamate 
• 109334-63-6 1-(3-Chloro-phenyl)-5-(2-nitro-phenyl)-3-phenyl-1H-pyrazole-4-carboxylic acid ethyl ester 
• 109334-56-7 1-(3-Chloro-phenyl)-5-(2-nitro-phenyl)-3-phenyl-1H-pyrazole-4-carboxylic acid methyl ester 
• 50802-12-5 1-(α-chlorobenzylidene)-2-(3-chlorophenyl)hydrazine 
• 109334-61-4 ethyl (2-nitrobenzoyl)benzoylacetate 
• 109334-68-1 1-(3-Chloro-phenyl)-3-phenyl-1,5-dihydro-pyrazolo[4,3-c]quinolin-4-one 
• 74-88-4 methyl iodide 

Relevant articles and documents

Cascade 1,3-dipolar Cycloaddition/SO2 extrusion approach for the rapid synthesis of tetraaryl-substituted pyrazoles with Aggregation Induced Emission characteristics

A highly efficient strategy was developed for the straightforward synthesis of tetraaryl-substituted pyrazoles. The cascade process consists of a regioselective 1,3-dipolar cycloaddition of benzosultam-3-ylidenes with nitrile imines and a subsequent elimination of SO2. The title compounds exhibit high fluorescence quantum yields and Aggregation Induced Emission (AIE) characteristics.

1,3-diarylpyrazolo[4,5-c]- and -[5,4-c]quinolin-4-ones. 4. Synthesis and specific inhibition of benzodiazepine receptor binding

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