Cas 1297310-03-2,7-hydroxy-2-imino-N'-[1-(5-methyl-2-phenyl-1H-imidazol-4-yl)ethylidene]-2H-chromene-3-carbohydrazide

1297310-03-2

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Basic information

Product Name: 7-hydroxy-2-imino-N'-[1-(5-methyl-2-phenyl-1H-imidazol-4-yl)ethylidene]-2H-chromene-3-carbohydrazide
Synonyms: 7-hydroxy-2-imino-N'-[1-(5-methyl-2-phenyl-1H-imidazol-4-yl)ethylidene]-2H-chromene-3-carbohydrazide
CAS NO:1297310-03-2
Molecular Formula:
Molecular Weight: 401.425
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: 7-hydroxy-2-imino-N'-[1-(5-methyl-2-phenyl-1H-imidazol-4-yl)ethylidene]-2H-chromene-3-carbohydrazide(CAS DataBase Reference)
NIST Chemistry Reference: 7-hydroxy-2-imino-N'-[1-(5-methyl-2-phenyl-1H-imidazol-4-yl)ethylidene]-2H-chromene-3-carbohydrazide(1297310-03-2)
EPA Substance Registry System: 7-hydroxy-2-imino-N'-[1-(5-methyl-2-phenyl-1H-imidazol-4-yl)ethylidene]-2H-chromene-3-carbohydrazide(1297310-03-2)

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: 1297310-03-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1297310-03-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,7,3,1 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1297310-03:
(9*1)+(8*2)+(7*9)+(6*7)+(5*3)+(4*1)+(3*0)+(2*0)+(1*3)=152
152 % 10 = 2
So 1297310-03-2 is a valid CAS Registry Number.

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1297310-03-2Relevant 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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