Cas 111425-17-3,N-(4-Chloro-phenyl)-N'-(4-methyl-benzyl)-N-(2-oxo-1,2-diphenyl-ethyl)-oxalamide

111425-17-3

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Basic information

Product Name: N-(4-Chloro-phenyl)-N'-(4-methyl-benzyl)-N-(2-oxo-1,2-diphenyl-ethyl)-oxalamide
Synonyms: N-(4-Chloro-phenyl)-N'-(4-methyl-benzyl)-N-(2-oxo-1,2-diphenyl-ethyl)-oxalamide
CAS NO:111425-17-3
Molecular Formula:
Molecular Weight: 496.993
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-(4-Chloro-phenyl)-N'-(4-methyl-benzyl)-N-(2-oxo-1,2-diphenyl-ethyl)-oxalamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(4-Chloro-phenyl)-N'-(4-methyl-benzyl)-N-(2-oxo-1,2-diphenyl-ethyl)-oxalamide(111425-17-3)
EPA Substance Registry System: N-(4-Chloro-phenyl)-N'-(4-methyl-benzyl)-N-(2-oxo-1,2-diphenyl-ethyl)-oxalamide(111425-17-3)

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: 111425-17-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 111425-17-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,4,2 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 111425-17:
(8*1)+(7*1)+(6*1)+(5*4)+(4*2)+(3*5)+(2*1)+(1*7)=73
73 % 10 = 3
So 111425-17-3 is a valid CAS Registry Number.

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111425-17-3Relevant academic research and scientific papers

Oxamic Acid Derivatives in Heterocyclic Synthesis: Preparation of 1,4-Oxazine and 1,2,4-Triazinooxadiazine Derivatives

Molina, P.,Tarraga, A.,Espinosa, A.,Lidon, M. J.

, p. 128 - 134 (2007/10/02)

A number of derivatives of the 1,4-oxazine ring system have been prepared by reaction of N-aryl-N-(α-phenylphenacyl)oxamoyl chlorides 1 with amines.Reaction of N-aroyl-N'-ethoxyoxalyl-phenylhydrazines 2 with unsubstituted amidrazones leads to functionaliz

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