Cas 1108616-39-2,6-(4-chlorophenylimino)-2,3-diphenyl-3,6-dihydropyrimidine-4,5-dicarboxylic acid dimethyl ester

1108616-39-2

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Basic information

Product Name: 6-(4-chlorophenylimino)-2,3-diphenyl-3,6-dihydropyrimidine-4,5-dicarboxylic acid dimethyl ester
Synonyms:
CAS NO:1108616-39-2
Molecular Formula:
Molecular Weight: 473.915
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: 6-(4-chlorophenylimino)-2,3-diphenyl-3,6-dihydropyrimidine-4,5-dicarboxylic acid dimethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 6-(4-chlorophenylimino)-2,3-diphenyl-3,6-dihydropyrimidine-4,5-dicarboxylic acid dimethyl ester(1108616-39-2)
EPA Substance Registry System: 6-(4-chlorophenylimino)-2,3-diphenyl-3,6-dihydropyrimidine-4,5-dicarboxylic acid dimethyl ester(1108616-39-2)

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: 1108616-39-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1108616-39-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,8,6,1 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1108616-39:
(9*1)+(8*1)+(7*0)+(6*8)+(5*6)+(4*1)+(3*6)+(2*3)+(1*9)=132
132 % 10 = 2
So 1108616-39-2 is a valid CAS Registry Number.

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1108616-39-2Relevant academic research and scientific papers

Investigations on the reactions of thioamides and related 1,3-diazabuta-1,3-dienes with dimethyl acetylenedicarboxylate: Synthesis of novel functionalized heterocycles

Marwaha, Alka,Sudan, Vishal,Mahajan, Mohinder P.

experimental part, p. 1087 - 1102 (2009/06/28)

The manuscript describes an investigation on the reaction pathways followed in the reactions of variedly substituted thioamides and the corresponding 1,3-diazabuta-1,3-dienes with dimethyl acetylene dicarboxylate. The mechanistic rationales for the reacti

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