Cas 1199554-94-3,1(4),3(4)-dioxa-1(3),3(3)-diphenyl-1,3(1,5)-diimidazo[1,5-a]quinoxalina-2(1,3)benzene-6,9-dioxacycloundecane

1199554-94-3

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Basic information

Product Name: 1⁽⁴⁾,3⁽⁴⁾-dioxa-1⁽³⁾,3⁽³⁾-diphenyl-1,3(1,5)-diimidazo[1,5-a]quinoxalina-2(1,3)benzene-6,9-dioxacycloundecane
Synonyms:
CAS NO:1199554-94-3
Molecular Formula:
Molecular Weight: 710.792
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⁽⁴⁾,3⁽⁴⁾-dioxa-1⁽³⁾,3⁽³⁾-diphenyl-1,3(1,5)-diimidazo[1,5-a]quinoxalina-2(1,3)benzene-6,9-dioxacycloundecane(CAS DataBase Reference)
NIST Chemistry Reference: 1⁽⁴⁾,3⁽⁴⁾-dioxa-1⁽³⁾,3⁽³⁾-diphenyl-1,3(1,5)-diimidazo[1,5-a]quinoxalina-2(1,3)benzene-6,9-dioxacycloundecane(1199554-94-3)
EPA Substance Registry System: 1⁽⁴⁾,3⁽⁴⁾-dioxa-1⁽³⁾,3⁽³⁾-diphenyl-1,3(1,5)-diimidazo[1,5-a]quinoxalina-2(1,3)benzene-6,9-dioxacycloundecane(1199554-94-3)

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: 1199554-94-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1199554-94-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,9,5,5 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1199554-94:
(9*1)+(8*1)+(7*9)+(6*9)+(5*5)+(4*5)+(3*4)+(2*9)+(1*4)=213
213 % 10 = 3
So 1199554-94-3 is a valid CAS Registry Number.

1199554-94-3Upstream product

1477-55-0 1,3-di(aminomethyl)benzene

1199554-94-3Downstream Products

1199554-94-3Relevant academic research and scientific papers

An efficient method for the synthesis of imidazo[1,5-a]quinoxalines from 3-acylquinoxalinones and benzylamines via a novel imidazoannulation

Mamedov, Vakhid A.,Kalinin, Aleksey A.,Balandina, Alsu A.,Rizvanov, Il'dar Kh.,Latypov, Shamil K.

, p. 9412 - 9420 (2009)

The reaction of 3-aroylquinoxalin-2(1H)-ones and their N-alkyl analogues with benzylamines in DMSO proceeds through an intermediate formation of N-(α-quinoxalinylbenzylydene)benzylamine, which when subjected to oxidative cyclocondensation gives imidazo[1,

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