85825-82-7

Basic information

• Product Name: 5-methoxycarbonyl-2,6-dimethyl-4-phenyl-1,4-dihydropyridine-3-carboxylic acid
• Synonyms: 5-methoxycarbonyl-2,6-dimethyl-4-phenyl-1,4-dihydropyridine-3-carboxylic acid
• CAS NO: 85825-82-7
• Molecular Weight: 287.315
• Mol File: 85825-82-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 5-methoxycarbonyl-2,6-dimethyl-4-phenyl-1,4-dihydropyridine-3-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 5-methoxycarbonyl-2,6-dimethyl-4-phenyl-1,4-dihydropyridine-3-carboxylic acid(85825-82-7)
• EPA Substance Registry System: 5-methoxycarbonyl-2,6-dimethyl-4-phenyl-1,4-dihydropyridine-3-carboxylic acid(85825-82-7)

Safety Data

• Hazardous Substances Data: 85825-82-7(Hazardous Substances Data)

Upstream product

• 138279-26-2 (+)-methyl pivaloyloxymethyl 1,4-dihydro-2,6-dimethyl-4-phenyl-3,5-pyridinedicarboxylate 
• 141600-86-4 1-Methoxymethyl-2,6-dimethyl-4-phenyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid 
• 138279-23-9 (+)-methyl pivaloyloxymethyl 1,4-dihydro-2,6-dimethyl-1-methoxymethyl-4-phenyl-3,5-pyridinedicarboxylate 
• 138279-17-1 1-Methoxymethyl-2,6-dimethyl-4-phenyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid mono-(2,2-dimethyl-propionyloxymethyl) ester 
• 138279-13-7 bis(pivaloyloxymethyl) 1,4-dihydro-1-(methoxymethyl)-2,6-dimethyl-4-phenyl-3,5-pyridinedicarboxylate 
• 70677-78-0 dimethyl 4-phenyl-1,4-dihydro-2,6-dimethylpyridine-3,5-dicarboxylate 
• 100-52-7 benzaldehyde 

Relevant articles and documents

Synthesis and photoluminescent properties of novel 1,4-dihydropyridine derivatives

Six new 1,4-dihydropyridine derivatives were synthesized, the UV-vis absorption and photoluminescence of these compounds were also studied. All the compounds exhibited strong blue emissions. (λem:436-451nm). The results showed that the absorption maxima of the compounds vary from 332 to 345nm depending on the group bonded to dihydropyridines rings.

Acyloxymethyl as an activating group in lipase-catalyzed enantioselective hydrolysis. A versatile approach to chiral 4-aryl-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylates

The first practical syntheses of chiral 4-aryl-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylates, which are attractive compounds as new calcium antagonists, were realized by lipase-catalyzed enantioselective hydrolysis of the acyloxymethyl esters. The monoesters obtained were revealed to have high optical purity and demonstrated to be useful chiral synthons.