Cas 1297309-76-2,2-{[1-(5-methyl-2-phenyl-1H-imidazol-4-yl)ethylidene]hydrazono}-4-phenyl-2,5-dihydrothiazole

1297309-76-2

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Basic information

Product Name: 2-{[1-(5-methyl-2-phenyl-1H-imidazol-4-yl)ethylidene]hydrazono}-4-phenyl-2,5-dihydrothiazole
Synonyms: 2-{[1-(5-methyl-2-phenyl-1H-imidazol-4-yl)ethylidene]hydrazono}-4-phenyl-2,5-dihydrothiazole
CAS NO:1297309-76-2
Molecular Formula:
Molecular Weight: 373.481
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-{[1-(5-methyl-2-phenyl-1H-imidazol-4-yl)ethylidene]hydrazono}-4-phenyl-2,5-dihydrothiazole(CAS DataBase Reference)
NIST Chemistry Reference: 2-{[1-(5-methyl-2-phenyl-1H-imidazol-4-yl)ethylidene]hydrazono}-4-phenyl-2,5-dihydrothiazole(1297309-76-2)
EPA Substance Registry System: 2-{[1-(5-methyl-2-phenyl-1H-imidazol-4-yl)ethylidene]hydrazono}-4-phenyl-2,5-dihydrothiazole(1297309-76-2)

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: 1297309-76-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1297309-76-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,7,3,0 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1297309-76:
(9*1)+(8*2)+(7*9)+(6*7)+(5*3)+(4*0)+(3*9)+(2*7)+(1*6)=192
192 % 10 = 2
So 1297309-76-2 is a valid CAS Registry Number.

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1297309-76-2Relevant academic research and scientific papers

Synthesis, antimicrobial, antioxidant, anti-hemolytic and cytotoxic evaluation of new imidazole-based heterocycles

Abdel-Wahab, Bakr F.,Awad, Ghada E.A.,Badria, Farid A.

, p. 1505 - 1511 (2011/05/06)

In the present work, 1-(5-methyl-2-phenyl-1H-imidazol-4-yl)ethanone 1 was prepared and used as a precursor for the synthesis of new thiazole, arylidiene and coumarin derivatives. The antimicrobial, antioxidant, anti-hemolytic, and cytotoxic activities of

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