Cas 154926-96-2,4-(1-Benzyl-4-nitro-imidazol-5-yl)-1,4-dihydro-2,6-dimethyl-pyridin-3,5-dicarbonsaeuredimethylester

154926-96-2

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Basic information

Product Name: 4-(1-Benzyl-4-nitro-imidazol-5-yl)-1,4-dihydro-2,6-dimethyl-pyridin-3,5-dicarbonsaeuredimethylester
Synonyms: 4-(1-Benzyl-4-nitro-imidazol-5-yl)-1,4-dihydro-2,6-dimethyl-pyridin-3,5-dicarbonsaeuredimethylester
CAS NO:154926-96-2
Molecular Formula:
Molecular Weight: 426.429
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: 4-(1-Benzyl-4-nitro-imidazol-5-yl)-1,4-dihydro-2,6-dimethyl-pyridin-3,5-dicarbonsaeuredimethylester(CAS DataBase Reference)
NIST Chemistry Reference: 4-(1-Benzyl-4-nitro-imidazol-5-yl)-1,4-dihydro-2,6-dimethyl-pyridin-3,5-dicarbonsaeuredimethylester(154926-96-2)
EPA Substance Registry System: 4-(1-Benzyl-4-nitro-imidazol-5-yl)-1,4-dihydro-2,6-dimethyl-pyridin-3,5-dicarbonsaeuredimethylester(154926-96-2)

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: 154926-96-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 154926-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,9,2 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 154926-96:
(8*1)+(7*5)+(6*4)+(5*9)+(4*2)+(3*6)+(2*9)+(1*6)=162
162 % 10 = 2
So 154926-96-2 is a valid CAS Registry Number.

154926-96-2Upstream product

154926-96-2Downstream Products

256530-68-4 4-(1-Benzyl-4-nitro-imidazol-5-yl)-2,6-dimethyl-pyridin-3,5-dicarbonsaeuredimethylester

154926-96-2Relevant academic research and scientific papers

Five-ring analogs of nifedipine. 3. Synthesis and reactions of 1,4-dihydropyridines with 4-(4-nitro-5-imidazolyl)-substituents

Goerlitzer,Klanck

, p. 814 - 819 (2007/10/03)

In the Hantzsch pyridine synthesis the 4-nitro-5-imidazolylcarbaldehydes 4 react with methyl 3-aminocrotonate or 3-aminocrotononitrile in acetic acid to yield the 1,4-dihydropyridines (DHP) 5 and 6. The corresponding pyridines 7 and 8 are obtained by oxid

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