Cas 95637-77-7,4-Imidazolidinecarboxamide, 3-benzoyl-4-[(4-bromophenyl)amino]-1-(4-methoxyphenyl)-5-methylene- N-phenyl-2-thioxo-

95637-77-7

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Basic information

Product Name: 4-Imidazolidinecarboxamide, 3-benzoyl-4-[(4-bromophenyl)amino]-1-(4-methoxyphenyl)-5-methylene- N-phenyl-2-thioxo-
Synonyms:
CAS NO:95637-77-7
Molecular Formula: C31H25BrN4O3S
Molecular Weight: 613.534
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-4-[(4-bromophenyl)amino]-1-(4-methoxyphenyl)-5-methylene- N-phenyl-2-thioxo-(CAS DataBase Reference)
NIST Chemistry Reference: 4-Imidazolidinecarboxamide, 3-benzoyl-4-[(4-bromophenyl)amino]-1-(4-methoxyphenyl)-5-methylene- N-phenyl-2-thioxo-(95637-77-7)
EPA Substance Registry System: 4-Imidazolidinecarboxamide, 3-benzoyl-4-[(4-bromophenyl)amino]-1-(4-methoxyphenyl)-5-methylene- N-phenyl-2-thioxo-(95637-77-7)

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: 95637-77-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 95637-77-7 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 95637-77:
(7*9)+(6*5)+(5*6)+(4*3)+(3*7)+(2*7)+(1*7)=177
177 % 10 = 7
So 95637-77-7 is a valid CAS Registry Number.

95637-77-7Upstream product

95637-77-7Downstream Products

95637-77-7Relevant 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 (1984)

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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