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5-(4-Methoxybenzyl)imidazo[1,5-a]quinoxalin-4(5H)-one is a complex organic compound belonging to the imidazoquinoxaline family. It features a quinoxaline core with an imidazole ring fused to it, and a 4-methoxybenzyl group attached to the 5-position. 5-(4-Methoxybenzyl)imidazo[1,5-a]quinoxalin-4(5H)-one is characterized by its molecular formula C18H15N3O2 and a molecular weight of 307.33 g/mol. It is known for its potential applications in medicinal chemistry, particularly as a building block for the synthesis of biologically active molecules. The compound's structure provides a platform for further functionalization and exploration of its properties in drug discovery and development.

221025-37-2

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221025-37-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 221025-37-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,1,0,2 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 221025-37:
(8*2)+(7*2)+(6*1)+(5*0)+(4*2)+(3*5)+(2*3)+(1*7)=72
72 % 10 = 2
So 221025-37-2 is a valid CAS Registry Number.

221025-37-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[(4-methoxyphenyl)methyl]imidazo[1,5-a]quinoxalin-4-one

1.2 Other means of identification

Product number -
Other names 5-(4-Methoxybenzyl)imidazo[1,5-a]quinoxalin-4(5H)-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:221025-37-2 SDS

221025-37-2Relevant academic research and scientific papers

De novo synthesis of imidazoles by visible-light-induced photocatalytic aerobic oxidation/[3+2] cycloaddition/aromatization cascade

Deng, Qiao-Hui,Zou, You-Quan,Lu, Liang-Qiu,Tang, Zi-Long,Chen, Jia-Rong,Xiao, Wen-Jing

supporting information, p. 2432 - 2435 (2014/10/15)

A visible-light-induced photocatalytic aerobic oxidation/[3+2] cycloaddition/aromatization cascade between secondary amines and isocyanides has been successfully developed. The reaction provides a general and efficient access to diversely substituted imidazoles and imidazo[1,5-a]quinoxalin-4(5 H)-ones in good yields under mild conditions.

Reaction of quinoxalin-2-ones with TosMIC reagent: Synthesis of imidazo[1,5-a]quinoxalin-4-ones

Chen, Ping,Barrish, Joel C.,Iwanowicz, Edwin,Lin, James,Bednarz, Mark S.,Chen, Bang-Chi

, p. 4293 - 4295 (2007/10/03)

Imidazo[1,5-a]quinoxalin-4-ones were prepared in four steps starting from 1,2-phenylenediamines using a new strategy for the construction of the ring system. A key step in this new method involves the reaction of quinoxalin-2-ones with TosMIC (tosylmethyl isocyanide).

Imidazoquinoxaline protein tyrosine kinase inhibitors

-

, (2008/06/13)

Novel imidazoquinoxalines and salts thereof, pharmaceutical compositions containing such compounds, and methods of using such compounds in the treatment of protein tyrosine kinase-associated disorders such as immunologic disorders.

Imidazoquinoxaline protein tyrosine kinase inhibitors

-

, (2008/06/13)

Novel imidazoquinoxalines and salts thereof, pharmaceutical compositions containing such compounds, and methods of using such compounds in the treatment of protein tyrosine kinase-associated disorders such as immunologic disorders.

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