138624-40-5

Basic information

• Product Name: 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-4-(1-phenylethyl)-, diethyl ester
• CAS NO: 138624-40-5
• Molecular Formula: C21H27NO4
• Molecular Weight: 357.45
• Mol File: 138624-40-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-4-(1-phenylethyl)-, diethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-4-(1-phenylethyl)-, diethyl ester(138624-40-5)
• EPA Substance Registry System: 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-4-(1-phenylethyl)-, diethyl ester(138624-40-5)

Safety Data

• Hazardous Substances Data: 138624-40-5(Hazardous Substances Data)

Upstream product

• 34713-70-7 2-Phenylpropanal 
• 141-97-9 ethyl acetoacetate 
• 41867-20-3 ethyl (E)-3-aminobut-2-enoate 
• 140429-22-7 N-(1-chloro-2-phenylpropyl)pyridinium chloride 

Downstream Products

• 951-85-9 (S)-methyldesoxybenzoin 
• 58751-83-0 1,2-diphenylpropan-1-one 
• 103130-61-6 (2R)-2-phenylpentan-3-one 
• 63801-22-9 2-phenylpentan-3-one 
• 65248-43-3 2-phenylhexan-3-one 
• 123696-10-6 7-phenyloctane-2,6-dione 
• 154554-67-3 1-phenyl-1-(2',2',6',6'-tetramethyl-1'-piperidinyloxy)ethane 
• 72256-08-7 1,4-diphenyl-1-pentanone 

Relevant articles and documents

Radical alkylation of: Para -quinone methides with 4-substituted Hantzsch esters/nitriles via organic photoredox catalysis

A novel photocatalytic protocol is herein described for the preparation of functionalized phenols via radical alkylation of para-quinone methides under transition-metal-free conditions. The reaction is external oxidant free and performed at ambient temperature upon visible light irradiation, allowing the access to various desired products in satisfactory yields. The readily available 4-alkyl-1,4-dihydropyridines serve as the effective alkyl radical precursors.

Novel syntheses of heterocycles with N-(1-haloalkyl)azinium halides. Part 2. Preparation of N-unsubstituted 1,4-dihydropyridines

N-(1-Chloroalkyl)pyridinium chlorides, prepared from thionyl chloride, pyridine, and aldehydes, readily react with enaminocarbonyl derivatives to yield 1,4-dihydropyridines under mild and neutral conditions.