Cas 146763-33-9,diethyl 4-(4-chlorophenyl)-1-(4-methoxyphenyl)-2,6-dimethyl-1,4-dihydro-3,5-pyridinedicarboxylate

146763-33-9

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Basic information

Product Name: diethyl 4-(4-chlorophenyl)-1-(4-methoxyphenyl)-2,6-dimethyl-1,4-dihydro-3,5-pyridinedicarboxylate
Synonyms: diethyl 4-(4-chlorophenyl)-1-(4-methoxyphenyl)-2,6-dimethyl-1,4-dihydro-3,5-pyridinedicarboxylate
CAS NO:146763-33-9
Molecular Formula: C26H28ClNO5
Molecular Weight: 469.95722
EINECS: N/A
Product Categories: N/A
Mol File: 146763-33-9.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: diethyl 4-(4-chlorophenyl)-1-(4-methoxyphenyl)-2,6-dimethyl-1,4-dihydro-3,5-pyridinedicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: diethyl 4-(4-chlorophenyl)-1-(4-methoxyphenyl)-2,6-dimethyl-1,4-dihydro-3,5-pyridinedicarboxylate(146763-33-9)
EPA Substance Registry System: diethyl 4-(4-chlorophenyl)-1-(4-methoxyphenyl)-2,6-dimethyl-1,4-dihydro-3,5-pyridinedicarboxylate(146763-33-9)

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: 146763-33-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 146763-33-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,7,6 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 146763-33:
(8*1)+(7*4)+(6*6)+(5*7)+(4*6)+(3*3)+(2*3)+(1*3)=149
149 % 10 = 9
So 146763-33-9 is a valid CAS Registry Number.

146763-33-9Upstream product

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146763-33-9Relevant articles and documents

Novel synthese of heterocycles with N-(1-haloalkyl)azinium halides. Part 5. Preparation of N-substituted 1,4-dihydropyridines

Vanden Eynde,Mayence,Maquestiau,Anders

, p. 3291 - 3304 (2007/10/02)

Thirty N-substituted Hantzsch 1,4-dihydropyridines were prepared under mild and neutral conditions from N-substituted enaminocarbonyl derivatives and aldehydes activated under the form of N-(1-chloroalkyl)pyridinium chlorides by means of thionyl chloride

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