Cas 41393-51-5,Propanedioic acid, [(chloroacetyl)amino][[4-chloro-2-(2-chlorobenzoyl)phenyl]azo]-, diethyl ester

41393-51-5

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Basic information

Product Name: Propanedioic acid, [(chloroacetyl)amino][[4-chloro-2-(2-chlorobenzoyl)phenyl]azo]-, diethyl ester
Synonyms:
CAS NO:41393-51-5
Molecular Formula: C22H20Cl3N3O6
Molecular Weight: 528.776
EINECS: N/A
Product Categories: N/A
Mol File: 41393-51-5.mol

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: Propanedioic acid, [(chloroacetyl)amino][[4-chloro-2-(2-chlorobenzoyl)phenyl]azo]-, diethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Propanedioic acid, [(chloroacetyl)amino][[4-chloro-2-(2-chlorobenzoyl)phenyl]azo]-, diethyl ester(41393-51-5)
EPA Substance Registry System: Propanedioic acid, [(chloroacetyl)amino][[4-chloro-2-(2-chlorobenzoyl)phenyl]azo]-, diethyl ester(41393-51-5)

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: 41393-51-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 41393-51-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,9 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 41393-51:
(7*4)+(6*1)+(5*3)+(4*9)+(3*3)+(2*5)+(1*1)=105
105 % 10 = 5
So 41393-51-5 is a valid CAS Registry Number.

41393-51-5Upstream product

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41393-51-5Relevant academic research and scientific papers

199. Azomalonic Ester Syntheses. Part I. One-Step Synthesis of Triazolobenzodiazepines from Azomalonates. Preparation of Novel Polyaza Tricycles from Diethyl (2-Chloroacetamido)malonate

Heckendorn, Roland

, p. 2118 - 2129 (1987)

A useful synthetic principle for the preparation of N-heterocycles consists in the base treatment of azomalonates carrying electrophilic centers in the side chain.Thus, pharmacologically active triazolobenzodiazepine-carboxamides can be prepared in o

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