Cas 90091-78-4,2-[(E)-1-Benzoyl-2-(4-chloro-phenyl)-vinylsulfanyl]-5-[1-phenyl-meth-(Z)-ylidene]-1,5-dihydro-imidazol-4-one

90091-78-4

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Basic information

Product Name: 2-[(E)-1-Benzoyl-2-(4-chloro-phenyl)-vinylsulfanyl]-5-[1-phenyl-meth-(Z)-ylidene]-1,5-dihydro-imidazol-4-one
Synonyms: 2-[(E)-1-Benzoyl-2-(4-chloro-phenyl)-vinylsulfanyl]-5-[1-phenyl-meth-(Z)-ylidene]-1,5-dihydro-imidazol-4-one
CAS NO:90091-78-4
Molecular Formula:
Molecular Weight: 444.941
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: 2-[(E)-1-Benzoyl-2-(4-chloro-phenyl)-vinylsulfanyl]-5-[1-phenyl-meth-(Z)-ylidene]-1,5-dihydro-imidazol-4-one(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(E)-1-Benzoyl-2-(4-chloro-phenyl)-vinylsulfanyl]-5-[1-phenyl-meth-(Z)-ylidene]-1,5-dihydro-imidazol-4-one(90091-78-4)
EPA Substance Registry System: 2-[(E)-1-Benzoyl-2-(4-chloro-phenyl)-vinylsulfanyl]-5-[1-phenyl-meth-(Z)-ylidene]-1,5-dihydro-imidazol-4-one(90091-78-4)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 90091-78-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 90091-78-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,0,9 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 90091-78:
(7*9)+(6*0)+(5*0)+(4*9)+(3*1)+(2*7)+(1*8)=124
124 % 10 = 4
So 90091-78-4 is a valid CAS Registry Number.

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90091-78-4Relevant academic research and scientific papers

REACTIONS OF 5-ARYLIDENE-2-THIOHYDANTOINS, SYNTHESIS OF NEW CONDENSED IMIDAZOTHIAZOLES

Daboun, Hamed A.,Abdel-Fattah, A. M.,Hussein, M. M.,Shalaby, A. F. A.

, p. 1001 - 1007 (2007/10/02)

5-Arylidene-2-thiohydantioins reacted with 2-bromopropionic acid or ethyl 2-bromobutanoate and phenacyl bromide yielded corresponding S-substituted mercapto acids or esters and S-phenacyl derivatives, respectively.Cyclization of these compounds resulted i

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