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32388-00-4

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32388-00-4 Usage

Description

2,3-DIMETHYL-6,7-DIMETHOXYQUINOXALINE, also known as 6,7-Dimethoxy-2,3-dimethyl-quinoxaline (CAS# 32388-00-4), is an organic compound characterized by its off-white to pale yellow solid appearance. It is primarily recognized for its utility in the field of organic synthesis, where it serves as a valuable building block for the creation of more complex molecules and compounds.

Uses

Used in Organic Synthesis:
2,3-DIMETHYL-6,7-DIMETHOXYQUINOXALINE is used as a synthetic building block for the development of various complex organic molecules. Its unique structure and functional groups make it a versatile component in the synthesis of a wide range of compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,3-DIMETHYL-6,7-DIMETHOXYQUINOXALINE is used as a key intermediate in the synthesis of novel drug candidates. Its incorporation into drug molecules can potentially enhance their pharmacological properties, such as potency, selectivity, and bioavailability, leading to the development of more effective therapeutic agents.
Used in Agrochemical Industry:
2,3-DIMETHYL-6,7-DIMETHOXYQUINOXALINE also finds application in the agrochemical industry, where it is utilized as a starting material for the synthesis of new pesticides, herbicides, and other crop protection agents. Its unique chemical properties can contribute to the development of more effective and environmentally friendly agrochemicals.
Used in Dye and Pigment Industry:
In the dye and pigment industry, 2,3-DIMETHYL-6,7-DIMETHOXYQUINOXALINE is used as a precursor for the synthesis of various dyes and pigments. Its chemical structure can be modified to produce a range of colors and shades, making it a valuable component in the development of new dyes and pigments for various applications, such as textiles, plastics, and printing inks.
Used in Material Science:
2,3-DIMETHYL-6,7-DIMETHOXYQUINOXALINE is also employed in the field of material science, where it can be used to develop new materials with unique properties. Its incorporation into polymers, for example, can lead to the creation of materials with enhanced thermal stability, electrical conductivity, or mechanical strength, depending on the specific application requirements.

Check Digit Verification of cas no

The CAS Registry Mumber 32388-00-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,8 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 32388-00:
(7*3)+(6*2)+(5*3)+(4*8)+(3*8)+(2*0)+(1*0)=104
104 % 10 = 4
So 32388-00-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H14N2O2/c1-7-8(2)14-10-6-12(16-4)11(15-3)5-9(10)13-7/h5-6H,1-4H3

32388-00-4SDS

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 6,7-dimethoxy-2,3-dimethylquinoxaline

1.2 Other means of identification

Product number -
Other names 6,7-Dimethoxy-2,3-dimethyl-chinoxalin

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:32388-00-4 SDS

32388-00-4Downstream Products

32388-00-4Relevant articles and documents

One-pot synthesis of quinoxalines from reductive coupling of 2-nitroanilines and 1,2-diketones using indium

Go, Ahra,Lee, Geunsoo,Kim, Jaeho,Bae, Seolhee,Lee, Byung Min,Kim, Byeong Hyo

, p. 1215 - 1226 (2015/03/04)

The one-pot reduction-cyclization of 2-nitroanilines and 1,2-diketones to give quinoxalines was investigated. Using indium and an appropriate acid such as acetic acid or indium(III) chloride, various quinoxaline derivatives including 2,3-dialkylquinoxalines, 2,3-diphenylquinoxalines, 2,3-di-2-thiophenylquinoxalines, 2,3-di(pyridin-2-yl)quinoxalines, and dibenzo[a,c]phenazines were synthesized in moderate to excellent yield.

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