Cas 144255-92-5,Dimethyl-carbamic acid 2-benzyl-4-cyano-1-oxo-1,5-dihydro-benzo[4,5]imidazo[1,2-a]pyridin-3-yl ester

144255-92-5

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Basic information

Product Name: Dimethyl-carbamic acid 2-benzyl-4-cyano-1-oxo-1,5-dihydro-benzo[4,5]imidazo[1,2-a]pyridin-3-yl ester
Synonyms:
CAS NO:144255-92-5
Molecular Formula:
Molecular Weight: 386.41
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: Dimethyl-carbamic acid 2-benzyl-4-cyano-1-oxo-1,5-dihydro-benzo[4,5]imidazo[1,2-a]pyridin-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Dimethyl-carbamic acid 2-benzyl-4-cyano-1-oxo-1,5-dihydro-benzo[4,5]imidazo[1,2-a]pyridin-3-yl ester(144255-92-5)
EPA Substance Registry System: Dimethyl-carbamic acid 2-benzyl-4-cyano-1-oxo-1,5-dihydro-benzo[4,5]imidazo[1,2-a]pyridin-3-yl ester(144255-92-5)

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: 144255-92-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 144255-92-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,2,5 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 144255-92:
(8*1)+(7*4)+(6*4)+(5*2)+(4*5)+(3*5)+(2*9)+(1*2)=125
125 % 10 = 5
So 144255-92-5 is a valid CAS Registry Number.

144255-92-5Upstream product

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144255-92-5Relevant academic research and scientific papers

Benzimidazole condensed ring systems 8 (1). Synthesis of some substituted 1-oxo-1H,5H-pyrido[1,2-a] benzimidazole-4-carbonitriles with anticipated antimicrobial activity

Badawey,Gohar

, p. 489 - 496 (2007/10/02)

As a part of research project on the syntheses of a number of pyrido[1,2-a] benzimidazole derivatives with possible antimicrobial activity, some 3-(chloro or morpholino)-acetyloxy (2,3), 3-(N,N-dimethylcarbamoyloxy) (4,5) and 3-tosyloxy-1-oxo-1H,5H-pyrido

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