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4,6-dimethoxy-2-methyl-5-nitropyrimidine is a heterocyclic organic compound with the molecular formula C7H8N2O4. It features a pyrimidine ring that is substituted with two methoxy groups, a methyl group, and a nitro group. 4,6-dimethoxy-2-methyl-5-nitropyrimidine is known for its potential biological activities and medicinal properties, making it a valuable component in various applications.

29939-34-2

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29939-34-2 Usage

Uses

Used in Organic Synthesis:
4,6-dimethoxy-2-methyl-5-nitropyrimidine is used as a building block in organic synthesis for the production of various drugs and agrochemicals. Its unique structure and functional groups make it a versatile intermediate in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
Due to its potential biological activities, 4,6-dimethoxy-2-methyl-5-nitropyrimidine is utilized in pharmaceutical research for the development of new drugs. Its presence in various drug candidates highlights its importance in the discovery and design of novel therapeutic agents.
Used in the Development of Novel Materials:
4,6-dimethoxy-2-methyl-5-nitropyrimidine has been studied for its potential applications in the development of novel materials. Its unique chemical properties and structural features make it a promising candidate for creating innovative materials with specific properties and applications.
Used as an Intermediate in the Synthesis of Dyes and Pigments:
In the chemical industry, 4,6-dimethoxy-2-methyl-5-nitropyrimidine is used as an intermediate in the synthesis of dyes and pigments. Its ability to form various functional groups and its compatibility with other chemical compounds make it a valuable component in the production of colorants for different applications.
Safety Precautions:
It is crucial to handle 4,6-dimethoxy-2-methyl-5-nitropyrimidine with caution, as it may have harmful effects on human health and the environment if not used properly. Adequate safety measures, such as wearing protective gear and working in well-ventilated areas, should be taken to minimize potential risks associated with this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 29939-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,9,3 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 29939-34:
(7*2)+(6*9)+(5*9)+(4*3)+(3*9)+(2*3)+(1*4)=162
162 % 10 = 2
So 29939-34-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H9N3O4/c1-4-8-6(13-2)5(10(11)12)7(9-4)14-3/h1-3H3

29939-34-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-Dimethoxy-2-methyl-5-nitropyrimidine

1.2 Other means of identification

Product number -
Other names EINECS 249-964-6

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:29939-34-2 SDS

29939-34-2Relevant academic research and scientific papers

Pyrimidine derivatives

-

, (2008/06/13)

The present invention relates to novel 5-(ω-substituted amino-alkanoyl amino)pyrimidine derivatives, processes for producing the derivatives, and pharmaceutical compositions containing said derivatives. The compounds in the present invention have potent effects of inhibiting ACAT activity and lowering serum cholesterol. The compounds of the present invention are extremely useful for the treatment and/or prevention of arteriosclerosis or hyperlipidemia.

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