Cas 256530-63-9,4-(1-Benzyl-2-methyl-4-nitro-imidazol-5-yl)-1,4-dihydro-2,6-dimethyl-pyridin-3,5-dicarbonsaeuredimethylester

256530-63-9

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Basic information

Product Name: 4-(1-Benzyl-2-methyl-4-nitro-imidazol-5-yl)-1,4-dihydro-2,6-dimethyl-pyridin-3,5-dicarbonsaeuredimethylester
Synonyms: 4-(1-Benzyl-2-methyl-4-nitro-imidazol-5-yl)-1,4-dihydro-2,6-dimethyl-pyridin-3,5-dicarbonsaeuredimethylester
CAS NO:256530-63-9
Molecular Formula:
Molecular Weight: 440.456
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-2-methyl-4-nitro-imidazol-5-yl)-1,4-dihydro-2,6-dimethyl-pyridin-3,5-dicarbonsaeuredimethylester(CAS DataBase Reference)
NIST Chemistry Reference: 4-(1-Benzyl-2-methyl-4-nitro-imidazol-5-yl)-1,4-dihydro-2,6-dimethyl-pyridin-3,5-dicarbonsaeuredimethylester(256530-63-9)
EPA Substance Registry System: 4-(1-Benzyl-2-methyl-4-nitro-imidazol-5-yl)-1,4-dihydro-2,6-dimethyl-pyridin-3,5-dicarbonsaeuredimethylester(256530-63-9)

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: 256530-63-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 256530-63-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,6,5,3 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 256530-63:
(8*2)+(7*5)+(6*6)+(5*5)+(4*3)+(3*0)+(2*6)+(1*3)=139
139 % 10 = 9
So 256530-63-9 is a valid CAS Registry Number.

256530-63-9Upstream product

256530-63-9Downstream Products

256530-69-5 4-(1-Benzyl-2-methyl-4-nitro-imidazol-5-yl)-2,6-dimethyl-pyridin-3,5-dicarbonsaeuredimethylester

256530-63-9Relevant 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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