Cas 1310489-53-2,N-(1-(2-azidophenyl)-2-(tert-butylamino)-2-oxoethyl)-N-(3-chlorophenyl)benzamide

1310489-53-2

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Basic information

Product Name: N-(1-(2-azidophenyl)-2-(tert-butylamino)-2-oxoethyl)-N-(3-chlorophenyl)benzamide
Synonyms: N-(1-(2-azidophenyl)-2-(tert-butylamino)-2-oxoethyl)-N-(3-chlorophenyl)benzamide
CAS NO:1310489-53-2
Molecular Formula:
Molecular Weight: 461.951
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-(1-(2-azidophenyl)-2-(tert-butylamino)-2-oxoethyl)-N-(3-chlorophenyl)benzamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(1-(2-azidophenyl)-2-(tert-butylamino)-2-oxoethyl)-N-(3-chlorophenyl)benzamide(1310489-53-2)
EPA Substance Registry System: N-(1-(2-azidophenyl)-2-(tert-butylamino)-2-oxoethyl)-N-(3-chlorophenyl)benzamide(1310489-53-2)

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: 1310489-53-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1310489-53-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,0,4,8 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1310489-53:
(9*1)+(8*3)+(7*1)+(6*0)+(5*4)+(4*8)+(3*9)+(2*5)+(1*3)=132
132 % 10 = 2
So 1310489-53-2 is a valid CAS Registry Number.

1310489-53-2Upstream product

1310489-53-2Downstream Products

1310489-86-1 N-tert-butyl-3-(3-chlorophenyl)-2-phenyl-3,4-dihydroquinazoline-4-carboxamide

1310489-53-2Relevant academic research and scientific papers

New efficient synthesis of 2,3,4-trisubstituted 3,4-dihydroquinazolines by a Ugi 4CC/Staudinger/aza-Wittig sequence

Zhong, Ying,Wang, Long,Ding, Ming-Wu

, p. 3714 - 3723 (2011)

A series of 2,3,4-trisubstituted 3,4-dihydroquinazoline 3 was prepared by intramolecular aza-Wittig reaction of amide carbonyl groups with methyldiphenyl iminophosphorane, which was obtained from a Ugi 4CC/Staudinger sequence. Further intramolecular Heck

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