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3-Amino-6-Methylpyrazin-2(1H)-one is a heterocyclic organic compound with the molecular formula C5H7N3O. It is a pyrazinone derivative featuring a methyl group substitution at the sixth position. 3-AMino-6-Methylpyrazin-2(1H)-one holds potential pharmaceutical applications, primarily as a building block in the synthesis of various pharmaceuticals. Its unique structure and properties make it a subject of interest in the fields of chemical and pharmaceutical research.

43029-20-5

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43029-20-5 Usage

Uses

Used in Pharmaceutical Industry:
3-Amino-6-Methylpyrazin-2(1H)-one is used as a chemical intermediate for the synthesis of pharmaceuticals. Its heterocyclic structure and functional groups make it a valuable component in the development of new drugs with specific therapeutic properties.
Used in Chemical Research:
3-Amino-6-Methylpyrazin-2(1H)-one is utilized as a research compound in chemical studies. Its unique structure allows scientists to explore its reactivity, stability, and potential interactions with other molecules, contributing to the advancement of chemical knowledge and the discovery of new applications.

Check Digit Verification of cas no

The CAS Registry Mumber 43029-20-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,0,2 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 43029-20:
(7*4)+(6*3)+(5*0)+(4*2)+(3*9)+(2*2)+(1*0)=85
85 % 10 = 5
So 43029-20-5 is a valid CAS Registry Number.

43029-20-5SDS

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 3-amino-6-methyl-1H-pyrazin-2-one

1.2 Other means of identification

Product number -
Other names -

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:43029-20-5 SDS

43029-20-5Downstream Products

43029-20-5Relevant academic research and scientific papers

Studies on pyrazines; part 30: Synthesis of aminopyrazines from azidopyrazines

Sato,Matsuura,Miwa

, p. 931 - 934 (2007/10/02)

Azidopyrazines do not undergo reduction by reagents that are effective for the preparation of alkyl- or arylamines from the azides because the heterocyclic azides exist in the bicyclic form of tetrazolo[1,5-a]pyrazines. Nevertheless, the conversion into aminopyrazines was achieved by hydrogenolysis in the presence of ammonium hydroxide and palladium-on-carbon or particularly by reduction with tin(II) chloride in methanolic hydrochloric acid, in 34-87% yields. To elucidate the successful progress of the reaction, the equilibrium of azide-atetrazole was examined by 1H NMR spectroscopy in various solvents.

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