1579293-08-5

Basic information

• Product Name: N-butyl-3-(4-chlorophenyl)-7,7-dimethyl-5-oxo-1,4,5,6,7,8-hexahydrocinnoline-4-carboxamide
• Synonyms: N-butyl-3-(4-chlorophenyl)-7,7-dimethyl-5-oxo-1,4,5,6,7,8-hexahydrocinnoline-4-carboxamide
• CAS NO: 1579293-08-5
• Molecular Weight: 387.909
• Mol File: 1579293-08-5.mol

Chemical Properties

• CAS DataBase Reference: N-butyl-3-(4-chlorophenyl)-7,7-dimethyl-5-oxo-1,4,5,6,7,8-hexahydrocinnoline-4-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-butyl-3-(4-chlorophenyl)-7,7-dimethyl-5-oxo-1,4,5,6,7,8-hexahydrocinnoline-4-carboxamide(1579293-08-5)
• EPA Substance Registry System: N-butyl-3-(4-chlorophenyl)-7,7-dimethyl-5-oxo-1,4,5,6,7,8-hexahydrocinnoline-4-carboxamide(1579293-08-5)

Safety Data

• Hazardous Substances Data: 1579293-08-5(Hazardous Substances Data)

Upstream product

• 1579292-89-9 2-(butylamino)-3-(4-chlorobenzoyl)-6,6-dimethyl-6,7-dihydrobenzofuran-4(5H)-one 
• 2769-64-4 n-butyl isonitrile 
• 4996-21-8 1-(4-chloro-phenyl)-2,2-dihydroxy-ethanone 
• 126-81-8 dimedone 

Relevant articles and documents

Efficient domino strategy for the synthesis of polyfunctionalized benzofuran-4(5 H)-ones and cinnoline-4-carboxamides

An efficient, three-component strategy for the improved synthesis of multifunctionalized 6,7-dihydrobenzofuran-4(5H)-ones under microwave irradiation in ethyl alcohol within short periods has been established. The synthesized benzofuran-4(5H)-ones have been readily converted into polyfunctionalized cinnoline-4-carboxamides by treating with hydrazine hydratein in the same solvent through a regioselective ring-opening of the furan. Tedious workup procedures can be avoided because of the direct precipitation of products from the reaction solution by water addition, thus rendering the two-steps process ecofriendly.