Cas 1456782-12-9,3-benzyl-N-(tert-butyl)-2-methyl-4-(4-methylbenzoyl)-4,5-dihydro-3H-1,4-benzodiazepine-5-carboxamide

1456782-12-9

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Basic information

Product Name: 3-benzyl-N-(tert-butyl)-2-methyl-4-(4-methylbenzoyl)-4,5-dihydro-3H-1,4-benzodiazepine-5-carboxamide
Synonyms: 3-benzyl-N-(tert-butyl)-2-methyl-4-(4-methylbenzoyl)-4,5-dihydro-3H-1,4-benzodiazepine-5-carboxamide
CAS NO:1456782-12-9
Molecular Formula:
Molecular Weight: 467.611
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-benzyl-N-(tert-butyl)-2-methyl-4-(4-methylbenzoyl)-4,5-dihydro-3H-1,4-benzodiazepine-5-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: 3-benzyl-N-(tert-butyl)-2-methyl-4-(4-methylbenzoyl)-4,5-dihydro-3H-1,4-benzodiazepine-5-carboxamide(1456782-12-9)
EPA Substance Registry System: 3-benzyl-N-(tert-butyl)-2-methyl-4-(4-methylbenzoyl)-4,5-dihydro-3H-1,4-benzodiazepine-5-carboxamide(1456782-12-9)

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: 1456782-12-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1456782-12-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,6,7,8 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1456782-12:
(9*1)+(8*4)+(7*5)+(6*6)+(5*7)+(4*8)+(3*2)+(2*1)+(1*2)=189
189 % 10 = 9
So 1456782-12-9 is a valid CAS Registry Number.

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1456782-12-9Relevant academic research and scientific papers

A simple and one-pot synthesis of 2,3,4,5-tetrasubstituted 4,5-dihydro-3H-1,4-benzodiazepines

Wang, Ying,Chen, Min,Ding, Ming-Wu

, p. 9056 - 9062 (2013/09/24)

2,3,4,5-Tetrasubstituted 4,5-dihydro-3H-1,4-benzodiazepines were synthesized in one-pot by a new sequential Ugi 4CC/Staudinger/aza-Wittig reaction, starting from easily accessible o-azidobenzaldehyde, α-amino ketone hydrochloride, isocyanide and carboxylic acid.

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