Cas 1360113-81-0,2-(N-benzyl-N-(tert-butyloxycarbonyl)amino)-N-(6-chloro-3-(3-chlorobenzoyl)pyridin-2-yl)acetamide

1360113-81-0

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Basic information

Product Name: 2-(N-benzyl-N-(tert-butyloxycarbonyl)amino)-N-(6-chloro-3-(3-chlorobenzoyl)pyridin-2-yl)acetamide
Synonyms: 2-(N-benzyl-N-(tert-butyloxycarbonyl)amino)-N-(6-chloro-3-(3-chlorobenzoyl)pyridin-2-yl)acetamide
CAS NO:1360113-81-0
Molecular Formula:
Molecular Weight: 514.408
EINECS: N/A
Product Categories: N/A
Mol File: 1360113-81-0.mol
Article Data: 1

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: 2-(N-benzyl-N-(tert-butyloxycarbonyl)amino)-N-(6-chloro-3-(3-chlorobenzoyl)pyridin-2-yl)acetamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-(N-benzyl-N-(tert-butyloxycarbonyl)amino)-N-(6-chloro-3-(3-chlorobenzoyl)pyridin-2-yl)acetamide(1360113-81-0)
EPA Substance Registry System: 2-(N-benzyl-N-(tert-butyloxycarbonyl)amino)-N-(6-chloro-3-(3-chlorobenzoyl)pyridin-2-yl)acetamide(1360113-81-0)

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: 1360113-81-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1360113-81-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,0,1,1 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1360113-81:
(9*1)+(8*3)+(7*6)+(6*0)+(5*1)+(4*1)+(3*3)+(2*8)+(1*1)=110
110 % 10 = 0
So 1360113-81-0 is a valid CAS Registry Number.

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1360113-81-0Relevant articles and documents

Novel access to 1,4-benzodiazepin-2-ones via the Buchwald reaction and application to the synthesis of novel heterocyclics

Salomé, Christophe,Schmitt, Martine,Bourguignon, Jean-Jacques

, p. 1033 - 1035 (2012/03/26)

A new two step strategy for the preparation of 1,4-benzodiazepin-2-ones has been developed starting from the 2-halogenobenzophenone under Buchwald conditions (Pd(OAc)2, XantPhos, Cs2CO3, dioxane 100 °C). This strategy has

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