Cas 1380583-91-4,3-(4-fluorophenyl)-8-oxo-7,8-dihydro-3H-imidazo[4,5-d]pyrrolo[3,2-f][1,3]diazepine-9-carbonitrile

1380583-91-4

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Basic information

Product Name: 3-(4-fluorophenyl)-8-oxo-7,8-dihydro-3H-imidazo[4,5-d]pyrrolo[3,2-f][1,3]diazepine-9-carbonitrile
Synonyms: 3-(4-fluorophenyl)-8-oxo-7,8-dihydro-3H-imidazo[4,5-d]pyrrolo[3,2-f][1,3]diazepine-9-carbonitrile
CAS NO:1380583-91-4
Molecular Formula:
Molecular Weight: 306.259
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: 3-(4-fluorophenyl)-8-oxo-7,8-dihydro-3H-imidazo[4,5-d]pyrrolo[3,2-f][1,3]diazepine-9-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 3-(4-fluorophenyl)-8-oxo-7,8-dihydro-3H-imidazo[4,5-d]pyrrolo[3,2-f][1,3]diazepine-9-carbonitrile(1380583-91-4)
EPA Substance Registry System: 3-(4-fluorophenyl)-8-oxo-7,8-dihydro-3H-imidazo[4,5-d]pyrrolo[3,2-f][1,3]diazepine-9-carbonitrile(1380583-91-4)

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: 1380583-91-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1380583-91-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,5,8 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1380583-91:
(9*1)+(8*3)+(7*8)+(6*0)+(5*5)+(4*8)+(3*3)+(2*9)+(1*1)=174
174 % 10 = 4
So 1380583-91-4 is a valid CAS Registry Number.

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1380583-91-4Relevant academic research and scientific papers

Synthesis and electrochemical evaluation of substituted imidazo[4,5-d]pyrrolo[3,2-f][1,3] diazepine scaffolds

Zaki, Magdi E.A.,Paula Bettencourt,Fernandes, Francisco M.,Fernanda Proen?a

, p. 4628 - 4634 (2012/08/08)

Substituted 4-(2,5-dihydro-1H-pyrrol-3-yl)-1H-imidazoles were prepared from 5-amino-1-aryl-4-cyanoformimidoylimidazoles and cyanoacetamide, under mild experimental conditions. The pyrrolyl-imidazoles were cyclized to the corresponding 7,8-dihydroimidazo[4

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