Cas 89990-63-6,Propanoic acid, 2-[[4,5-dihydro-4-oxo-5-(phenylmethylene)-1H-imidazol-2-yl]thio]-

89990-63-6

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Basic information

Product Name: Propanoic acid, 2-[[4,5-dihydro-4-oxo-5-(phenylmethylene)-1H-imidazol-2-yl]thio]-
Synonyms:
CAS NO:89990-63-6
Molecular Formula: C13H12N2O3S
Molecular Weight: 276.316
EINECS: N/A
Product Categories: N/A
Mol File: 89990-63-6.mol
Article Data: 1

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: Propanoic acid, 2-[[4,5-dihydro-4-oxo-5-(phenylmethylene)-1H-imidazol-2-yl]thio]-(CAS DataBase Reference)
NIST Chemistry Reference: Propanoic acid, 2-[[4,5-dihydro-4-oxo-5-(phenylmethylene)-1H-imidazol-2-yl]thio]-(89990-63-6)
EPA Substance Registry System: Propanoic acid, 2-[[4,5-dihydro-4-oxo-5-(phenylmethylene)-1H-imidazol-2-yl]thio]-(89990-63-6)

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: 89990-63-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 89990-63-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,9,9 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 89990-63:
(7*8)+(6*9)+(5*9)+(4*9)+(3*0)+(2*6)+(1*3)=206
206 % 10 = 6
So 89990-63-6 is a valid CAS Registry Number.

89990-63-6Upstream product

89990-63-6Downstream Products

89990-67-0 5-benzylidene-2-methyl-2,3,5,6-tetrahydroimidazo<2,1-b>thiazol-3,6-dione

89990-63-6Relevant articles and documents

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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