Cas 30131-53-4,diethyl 1-benzyl-4-{4-nitrophenyl}-2,6-dimethyl-1,4-dihydro-3,5-pyridinedicarboxylate

30131-53-4

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Basic information

Product Name: diethyl 1-benzyl-4-{4-nitrophenyl}-2,6-dimethyl-1,4-dihydro-3,5-pyridinedicarboxylate
Synonyms: diethyl 1-benzyl-4-{4-nitrophenyl}-2,6-dimethyl-1,4-dihydro-3,5-pyridinedicarboxylate
CAS NO:30131-53-4
Molecular Formula: C₂₆H₂₈N₂O₆
Molecular Weight: 464.51032
EINECS: N/A
Product Categories: N/A
Mol File: 30131-53-4.mol

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 1-benzyl-4-{4-nitrophenyl}-2,6-dimethyl-1,4-dihydro-3,5-pyridinedicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: diethyl 1-benzyl-4-{4-nitrophenyl}-2,6-dimethyl-1,4-dihydro-3,5-pyridinedicarboxylate(30131-53-4)
EPA Substance Registry System: diethyl 1-benzyl-4-{4-nitrophenyl}-2,6-dimethyl-1,4-dihydro-3,5-pyridinedicarboxylate(30131-53-4)

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: 30131-53-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 30131-53-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,1,3 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 30131-53:
(7*3)+(6*0)+(5*1)+(4*3)+(3*1)+(2*5)+(1*3)=54
54 % 10 = 4
So 30131-53-4 is a valid CAS Registry Number.

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30131-53-4Relevant academic research and scientific papers

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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