Cas 1147743-56-3,3-(2-(acetylamino)propanoyl)-1-(4-ethoxycarbonylphenyl)-3-methyltriazene

1147743-56-3

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Basic information

Product Name: 3-(2-(acetylamino)propanoyl)-1-(4-ethoxycarbonylphenyl)-3-methyltriazene
Synonyms: 3-(2-(acetylamino)propanoyl)-1-(4-ethoxycarbonylphenyl)-3-methyltriazene
CAS NO:1147743-56-3
Molecular Formula:
Molecular Weight: 320.348
EINECS: N/A
Product Categories: N/A
Mol File: 1147743-56-3.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: 3-(2-(acetylamino)propanoyl)-1-(4-ethoxycarbonylphenyl)-3-methyltriazene(CAS DataBase Reference)
NIST Chemistry Reference: 3-(2-(acetylamino)propanoyl)-1-(4-ethoxycarbonylphenyl)-3-methyltriazene(1147743-56-3)
EPA Substance Registry System: 3-(2-(acetylamino)propanoyl)-1-(4-ethoxycarbonylphenyl)-3-methyltriazene(1147743-56-3)

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: 1147743-56-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1147743-56-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,7,7,4 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1147743-56:
(9*1)+(8*1)+(7*4)+(6*7)+(5*7)+(4*4)+(3*3)+(2*5)+(1*6)=163
163 % 10 = 3
So 1147743-56-3 is a valid CAS Registry Number.

1147743-56-3Upstream product

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1147743-56-3Relevant articles and documents

Towards an efficient prodrug of the alkylating metabolite monomethyltriazene: Synthesis and stability of N-acylamino acid derivatives of triazenes

Perry, Maria de Jesus,Carvalho, Emilia,Rosa, Eduarda,Iley, Jim

experimental part, p. 1049 - 1056 (2009/08/14)

A series of 3-[α-(acylamino)acyl]-1-aryl-3-methyltriazenes 6a-l, potential cytotoxic triazene prodrugs, were synthesised by coupling 1-aryl-3-methyltriazenes to N-acylamino acids. Their hydrolysis was studied in isotonic pH 7.4 phosphate buffer and in hum

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