Cas 95637-75-5,4-Imidazolidinecarboxamide, 3-benzoyl-1-(4-ethoxyphenyl)-5-methylene-N-phenyl-4-(phenylamino)-2- thioxo-

95637-75-5

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Basic information

Product Name: 4-Imidazolidinecarboxamide, 3-benzoyl-1-(4-ethoxyphenyl)-5-methylene-N-phenyl-4-(phenylamino)-2- thioxo-
Synonyms:
CAS NO:95637-75-5
Molecular Formula: C32H28N4O3S
Molecular Weight: 548.665
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: 4-Imidazolidinecarboxamide, 3-benzoyl-1-(4-ethoxyphenyl)-5-methylene-N-phenyl-4-(phenylamino)-2- thioxo-(CAS DataBase Reference)
NIST Chemistry Reference: 4-Imidazolidinecarboxamide, 3-benzoyl-1-(4-ethoxyphenyl)-5-methylene-N-phenyl-4-(phenylamino)-2- thioxo-(95637-75-5)
EPA Substance Registry System: 4-Imidazolidinecarboxamide, 3-benzoyl-1-(4-ethoxyphenyl)-5-methylene-N-phenyl-4-(phenylamino)-2- thioxo-(95637-75-5)

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: 95637-75-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 95637-75-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,6,3 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 95637-75:
(7*9)+(6*5)+(5*6)+(4*3)+(3*7)+(2*7)+(1*5)=175
175 % 10 = 5
So 95637-75-5 is a valid CAS Registry Number.

95637-75-5Upstream product

95637-75-5Downstream Products

95637-75-5Relevant academic research and scientific papers

CONJUGATED SCHIFF'S BASES.20. CYCLOADDITION OF HETEROCUMULENES TO SOME 1,3-HETERODIENES INVOLVING UNUSUAL ASSISTANCE OF METHYL GROUP

Moskal, Janusz

, p. 4447 - 4454 (2007/10/02)

Highly substituted 1,4-diazabutadienes react with aroyl isothiocyanates in a 1,3-dipolar cycloaddition node yielding five-membered thiohydantoin-type heterocycles.The cycloaddition is accompanied by 1,4 shift of hydrogen from a methyl group attached to C2 of the 1,4-diazabutadiene moiety.The mechanism of this reaction is discussed in comparison with similar cycloadditions with aryl isocyanates.

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