Cas 1428342-38-4,N-cyclohexyl-4,5-dihydro-5-(2,4-dinitrophenyl)-1,2,3-triazolo[1,5-a][1,4]benzodiazepine-6-carboxamide

1428342-38-4

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Basic information

Product Name: N-cyclohexyl-4,5-dihydro-5-(2,4-dinitrophenyl)-1,2,3-triazolo[1,5-a][1,4]benzodiazepine-6-carboxamide
Synonyms: N-cyclohexyl-4,5-dihydro-5-(2,4-dinitrophenyl)-1,2,3-triazolo[1,5-a][1,4]benzodiazepine-6-carboxamide
CAS NO:1428342-38-4
Molecular Formula:
Molecular Weight: 477.48
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: N-cyclohexyl-4,5-dihydro-5-(2,4-dinitrophenyl)-1,2,3-triazolo[1,5-a][1,4]benzodiazepine-6-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: N-cyclohexyl-4,5-dihydro-5-(2,4-dinitrophenyl)-1,2,3-triazolo[1,5-a][1,4]benzodiazepine-6-carboxamide(1428342-38-4)
EPA Substance Registry System: N-cyclohexyl-4,5-dihydro-5-(2,4-dinitrophenyl)-1,2,3-triazolo[1,5-a][1,4]benzodiazepine-6-carboxamide(1428342-38-4)

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: 1428342-38-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1428342-38-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,8,3,4 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1428342-38:
(9*1)+(8*4)+(7*2)+(6*8)+(5*3)+(4*4)+(3*2)+(2*3)+(1*8)=154
154 % 10 = 4
So 1428342-38-4 is a valid CAS Registry Number.

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1428342-38-4Relevant academic research and scientific papers

Synthesis of novel fused 4,5-dihydro-1,2,3-triazolo[1,5-a][1,4] benzodiazepine derivatives via four-component Ugi-Smiles-type reaction

Saeedi, Mina,Mahdavi, Mohammad,Foroumadi, Alireza,Shafiee, Abbas

, p. 3506 - 3510 (2013)

Using 2-azidobenzaldehyde and propargylamine in a Ugi-Smiles coupling gave easy access to 4,5-dihydro-1,2,3-triazolo[1,5-a][1,4]benzodiazepine derivatives. This novel approach is based on the reaction between 2-azidobenzaldehyde, propargylamine, isocyanides, and nitrophenols in methanol under reflux conditions without using additional reagents or catalysts.

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