Cas 114957-73-2,5-Cyano-6-methyl-2-(2-oxo-2-phenyl-ethyl)-4-(2-trifluoromethyl-phenyl)-1,4-dihydro-pyridine-3-carboxylic acid ethyl ester

114957-73-2

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Basic information

Product Name: 5-Cyano-6-methyl-2-(2-oxo-2-phenyl-ethyl)-4-(2-trifluoromethyl-phenyl)-1,4-dihydro-pyridine-3-carboxylic acid ethyl ester
Synonyms:
CAS NO:114957-73-2
Molecular Formula:
Molecular Weight: 454.449
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 5-Cyano-6-methyl-2-(2-oxo-2-phenyl-ethyl)-4-(2-trifluoromethyl-phenyl)-1,4-dihydro-pyridine-3-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 5-Cyano-6-methyl-2-(2-oxo-2-phenyl-ethyl)-4-(2-trifluoromethyl-phenyl)-1,4-dihydro-pyridine-3-carboxylic acid ethyl ester(114957-73-2)
EPA Substance Registry System: 5-Cyano-6-methyl-2-(2-oxo-2-phenyl-ethyl)-4-(2-trifluoromethyl-phenyl)-1,4-dihydro-pyridine-3-carboxylic acid ethyl ester(114957-73-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 114957-73-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 114957-73-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,9,5 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 114957-73:
(8*1)+(7*1)+(6*4)+(5*9)+(4*5)+(3*7)+(2*7)+(1*3)=142
142 % 10 = 2
So 114957-73-2 is a valid CAS Registry Number.

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114957-73-2Relevant academic research and scientific papers

2-(2-Aryl-2-oxoethylidene)-1,2,3,4-tetrahydropyridines. Novel isomers of 1,4-dihydropyridine calcium channel blockers

Taylor,Badger,Steffen,Haleen,Pugsley,Shih,Weishaar

, p. 1659 - 1664 (2007/10/02)

The title compounds are novel double bond isomers of 1,4-dihydropyridine-type calcium channel blockers (CCB). These derivatives were prepared by using the Hantzsch dihydropyridine synthesis. The assignment of structure was based on spectroscopic data and

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