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82032-74-4

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82032-74-4 Usage

Molecular Structure

A complex structure with a tetrahydropyrido[2,3-b]quinoxalin-5-ium core.

Methyl Group

A methyl group attached to the nitrogen atom in the core structure.

Oxo (Carbonyl) Groups

Two oxo groups present at positions 2 and 5 on the core structure.

Potential Applications

May have pharmaceutical or medicinal applications due to its unique structure.

Interaction with Biological Systems

The complex structure could potentially interact with biological systems in meaningful ways.

Further Research

Additional research and analysis are required to fully understand the properties and potential uses of this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 82032-74-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,3 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82032-74:
(7*8)+(6*2)+(5*0)+(4*3)+(3*2)+(2*7)+(1*4)=104
104 % 10 = 4
So 82032-74-4 is a valid CAS Registry Number.

82032-74-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-5-oxidopyrido[3,2-b]quinoxalin-5-ium-2-one

1.2 Other means of identification

Product number -
Other names Pyrido[2,3-b]quinoxalin-2(1H)-one,1-methyl-,5-oxide

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:82032-74-4 SDS

82032-74-4Downstream Products

82032-74-4Relevant articles and documents

Pyridoquinoxaline N-Oxides. 1. A New Class of Antitrichomonal Agents

Glazer, Edward A.,Chappel, Larry R.

, p. 766 - 769 (2007/10/02)

An aspect of our work with quinoxaline 1,4-dioxides involved the synthesis and reactivity of (quinoxalin-2-yl)acrylonitrile 1,4-dioxide.We have found that treatment of a methanolic solution of this unsaturated nitrile (cis or trans) with primary alkylamin

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