Cas 296889-23-1,1-(α-2-oxo-1,2-dihydro-3-quinoxalinyl)benzylthio-3-phenylimidazo[1,5-a]quinoxalin-4(5H)-one

296889-23-1

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Basic information

Product Name: 1-(α-2-oxo-1,2-dihydro-3-quinoxalinyl)benzylthio-3-phenylimidazo[1,5-a]quinoxalin-4(5H)-one
Synonyms:
CAS NO:296889-23-1
Molecular Formula:
Molecular Weight: 527.606
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: 1-(α-2-oxo-1,2-dihydro-3-quinoxalinyl)benzylthio-3-phenylimidazo[1,5-a]quinoxalin-4(5H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-(α-2-oxo-1,2-dihydro-3-quinoxalinyl)benzylthio-3-phenylimidazo[1,5-a]quinoxalin-4(5H)-one(296889-23-1)
EPA Substance Registry System: 1-(α-2-oxo-1,2-dihydro-3-quinoxalinyl)benzylthio-3-phenylimidazo[1,5-a]quinoxalin-4(5H)-one(296889-23-1)

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: 296889-23-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 296889-23-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,6,8,8 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 296889-23:
(8*2)+(7*9)+(6*6)+(5*8)+(4*8)+(3*9)+(2*2)+(1*3)=221
221 % 10 = 1
So 296889-23-1 is a valid CAS Registry Number.

296889-23-1Upstream product

124831-91-0 3-(α-chlorobenzyl)-1,2-dihydroxyquinoxalin-2-one

296889-23-1Downstream Products

296889-23-1Relevant academic research and scientific papers

Imidazo[1,5-a]- and thiazolo[3,4-a]-Quinoxalines based on 3-(α-thiocyano-benzyl)quinoxalin-2(1H)-one

Mamedov,Kalinin,Rizvanov,Azancheev,Efremov,Levin

, p. 1121 - 1129 (2002)

When 3-(α-thiocyanobenzyl-2(1H)-one is heated, competing processes of [a]-annelation of the imidazole or thiazole rings occurs with formation of imidazo[1,5-a]- and thiazolo[3,4-a]quinoxalin-4(5H)-ones.

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