Cas 1297492-99-9,ethyl 5-oxo-2,4-di(4-methylphenyl)-2,5-dihydro-1H-imidazol-2-carboxylate

1297492-99-9

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Basic information

Product Name: ethyl 5-oxo-2,4-di(4-methylphenyl)-2,5-dihydro-1H-imidazol-2-carboxylate
Synonyms: ethyl 5-oxo-2,4-di(4-methylphenyl)-2,5-dihydro-1H-imidazol-2-carboxylate
CAS NO:1297492-99-9
Molecular Formula:
Molecular Weight: 336.39
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: ethyl 5-oxo-2,4-di(4-methylphenyl)-2,5-dihydro-1H-imidazol-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 5-oxo-2,4-di(4-methylphenyl)-2,5-dihydro-1H-imidazol-2-carboxylate(1297492-99-9)
EPA Substance Registry System: ethyl 5-oxo-2,4-di(4-methylphenyl)-2,5-dihydro-1H-imidazol-2-carboxylate(1297492-99-9)

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: 1297492-99-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1297492-99-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,7,4,9 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1297492-99:
(9*1)+(8*2)+(7*9)+(6*7)+(5*4)+(4*9)+(3*2)+(2*9)+(1*9)=219
219 % 10 = 9
So 1297492-99-9 is a valid CAS Registry Number.

1297492-99-9Upstream product

15674-78-9 (+/-)-α-bromo-p-tolylacetic acid ethyl ester

1297492-99-9Downstream Products

1297492-99-9Relevant academic research and scientific papers

A one-pot preparation of 5-oxo 2,4-disubstituted 2,5-dihydro-1 H -imidazol-2-carboxylates from α-bromo esters

Ciez, Dariusz,Svetlik, Jan

supporting information; experimental part, p. 315 - 318 (2011/03/23)

Nucleophilic substitution of a bromine atom by the azide group in aryl- and heteroaryl -α- bromoacetates triggers cascade reactions leading to imidazolin-5-ones formation. The α-azidoacetate intermediates undergo a transformation into non-isolable 2-imino

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