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1H-Imidazo[4,5-f]quinoxaline,2-methyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87967-72-4

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87967-72-4 Usage

Structure

Heterocyclic aromatic compound with an imidazole ring fused to a quinoxaline ring and a methyl group attached at the 2-position of the imidazole ring.

Properties

Potential applications in the field of medicinal chemistry and pharmaceuticals due to possible biological activity.

Research status

Further research is needed to fully understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 87967-72-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,9,6 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 87967-72:
(7*8)+(6*7)+(5*9)+(4*6)+(3*7)+(2*7)+(1*2)=204
204 % 10 = 4
So 87967-72-4 is a valid CAS Registry Number.

87967-72-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-1H-imidazo<4,5-f>quinoxaline

1.2 Other means of identification

Product number -
Other names 2-methyl-1H-imidazo[4,5-f]quinoxaline

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:87967-72-4 SDS

87967-72-4Downstream Products

87967-72-4Relevant academic research and scientific papers

Synthesis of 2-Sustituted 1H-Imidazoquinoxalines

Kishan Rao, S.,Pandu Ranga Reddy, A.,Veerangaiah, V.

, p. 960 - 961 (2007/10/02)

Condensation of 5,6-diaminoquinoxaline (I) with aliphatic and aromatic acids under catalytic and thermal conditions yields the corresponding 2-alkyl/aryl-1H-imidazoquinoxalines (III).

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