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35676-71-2

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35676-71-2 Usage

Bicyclic heterocyclic compound

quinoxalinone derivative

Substitution

3-methoxy group added to the quinoxalinone ring

Potential applications

medicinal chemistry, pharmaceutical research, drug discovery and development

Properties

interesting pharmacological and biological properties

Usage

building block for the synthesis of more complex organic molecules

Unique structure

makes it an interesting target for further study

Check Digit Verification of cas no

The CAS Registry Mumber 35676-71-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,6,7 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 35676-71:
(7*3)+(6*5)+(5*6)+(4*7)+(3*6)+(2*7)+(1*1)=142
142 % 10 = 2
So 35676-71-2 is a valid CAS Registry Number.

35676-71-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methoxy-1H-quinoxalin-2-one

1.2 Other means of identification

Product number -
Other names 3-Methoxy-chinoxalin-2-on

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:35676-71-2 SDS

35676-71-2Downstream Products

35676-71-2Relevant articles and documents

Synthesis of 3-methoxy-quinoxalin-2-ones from methyl trimethoxyacetate and phenylenediamines

Venable, Jennifer D.,Kindrachuk, David E.,Peterson, Matthew L.,Edwards, James P.

, p. 337 - 339 (2010)

Treatment of phenylenediamines with methyl trimethoxyacetate led to the formation of 3-methoxy-quinoxalin-2-ones with the assistance of lanthanide-based Lewis acids.

Quinoxaline compounds

-

Page/Page column 13, (2008/06/13)

Quinoxaline compounds, compositions, methods of making them, and methods of using them in leukocyte recruitment inhibition, in modulating an H4 receptor, and in treating conditions such as inflammation, H4 receptor-mediated conditions, and related conditions.

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