Cas 70008-27-4,1,2,6-trimethyl-4-<i>p</i>-tolyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid diethyl ester

70008-27-4

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Basic information

Product Name: 1,2,6-trimethyl-4-p-tolyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid diethyl ester
Synonyms: 1,2,6-trimethyl-4-p-tolyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid diethyl ester
CAS NO:70008-27-4
Molecular Formula:
Molecular Weight: 357.45
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: 1,2,6-trimethyl-4-p-tolyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid diethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1,2,6-trimethyl-4-p-tolyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid diethyl ester(70008-27-4)
EPA Substance Registry System: 1,2,6-trimethyl-4-p-tolyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid diethyl ester(70008-27-4)

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: 70008-27-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 70008-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,0,0 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 70008-27:
(7*7)+(6*0)+(5*0)+(4*0)+(3*8)+(2*2)+(1*7)=84
84 % 10 = 4
So 70008-27-4 is a valid CAS Registry Number.

70008-27-4Upstream product

70008-27-4Downstream Products

84021-32-9 3,5-Bis-ethoxycarbonyl-1,2,6-trimethyl-4-p-tolyl-pyridinium

70008-27-4Relevant 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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