Cas 1586800-27-2,N-butyl-5-(4-methoxybenzyl)-6-oxo-5,6-dihydro-4H-benzo[f]imidazo[1,5-a][1,4]diazepine-4-carboxamide

1586800-27-2

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Basic information

Product Name: N-butyl-5-(4-methoxybenzyl)-6-oxo-5,6-dihydro-4H-benzo[f]imidazo[1,5-a][1,4]diazepine-4-carboxamide
Synonyms: N-butyl-5-(4-methoxybenzyl)-6-oxo-5,6-dihydro-4H-benzo[f]imidazo[1,5-a][1,4]diazepine-4-carboxamide
CAS NO:1586800-27-2
Molecular Formula:
Molecular Weight: 418.495
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-butyl-5-(4-methoxybenzyl)-6-oxo-5,6-dihydro-4H-benzo[f]imidazo[1,5-a][1,4]diazepine-4-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: N-butyl-5-(4-methoxybenzyl)-6-oxo-5,6-dihydro-4H-benzo[f]imidazo[1,5-a][1,4]diazepine-4-carboxamide(1586800-27-2)
EPA Substance Registry System: N-butyl-5-(4-methoxybenzyl)-6-oxo-5,6-dihydro-4H-benzo[f]imidazo[1,5-a][1,4]diazepine-4-carboxamide(1586800-27-2)

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: 1586800-27-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1586800-27-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,6,8,0 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1586800-27:
(9*1)+(8*5)+(7*8)+(6*6)+(5*8)+(4*0)+(3*0)+(2*2)+(1*7)=192
192 % 10 = 2
So 1586800-27-2 is a valid CAS Registry Number.

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1586800-27-2Relevant academic research and scientific papers

Microwave-assisted synthesis of 4H-benzo[f]imidazo[1,4]diazepin-6-ones via a post-Ugi copper-catalyzed intramolecular Ullmann coupling

Li, Zhenghua,Legras, Laetitia,Kumar, Amit,Vachhani, Dipak D.,Sharma, Sunil K.,Parmar, Virinder S.,Van Der Eycken, Erik V.

supporting information, p. 2070 - 2074 (2014/04/03)

An efficient post-Ugi copper-catalyzed intramolecular Ullmann coupling strategy has been elaborated for the diversity-oriented synthesis of 4H-benzo[f]imidazo[1,4]diazepin-6-ones and the scope and limitations of this protocol are investigated.

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