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88394-05-2

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88394-05-2 Usage

Description

Pyrazinecarboxamide, 3,4-dihydro-5-methyl-3-oxo(9CI) is a chemical compound with the molecular formula C6H8N2O2. It is a derivative of pyrazinecarboxamide, and is also known as 3,4-dihydro-5-methyl-3-oxo-pyrazine-2-carboxamide. Pyrazinecarboxamide, 3,4-dihydro-5-methyl-3-oxo(9CI) has potential industrial and pharmaceutical applications, particularly in the field of organic synthesis. It may also possess biological activities and pharmaceutical properties that make it useful in the development of new drugs. Further study and investigation are required to determine the specific uses and properties of this chemical.

Uses

Used in Organic Synthesis:
Pyrazinecarboxamide, 3,4-dihydro-5-methyl-3-oxo(9CI) is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for the formation of diverse chemical products, making it a valuable component in the development of new materials and pharmaceuticals.
Used in Pharmaceutical Development:
Due to its potential biological activities and pharmaceutical properties, Pyrazinecarboxamide, 3,4-dihydro-5-methyl-3-oxo(9CI) is used as a starting material for the development of new drugs. Its structure can be modified to create novel compounds with potential therapeutic applications, contributing to advancements in medicine and healthcare.
Used in Research and Development:
Pyrazinecarboxamide, 3,4-dihydro-5-methyl-3-oxo(9CI) is utilized in research and development settings to study its properties and potential applications. Scientists and researchers explore its chemical behavior, reactivity, and interactions with other compounds to gain insights into its possible uses and benefits.
Note: The specific applications and industries for Pyrazinecarboxamide, 3,4-dihydro-5-methyl-3-oxo(9CI) are not provided in the materials. The uses listed above are inferred based on the general potential of the compound as mentioned in the provided materials. Further research and investigation would be necessary to confirm these applications and identify specific industries where the compound is utilized.

Check Digit Verification of cas no

The CAS Registry Mumber 88394-05-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,9 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 88394-05:
(7*8)+(6*8)+(5*3)+(4*9)+(3*4)+(2*0)+(1*5)=172
172 % 10 = 2
So 88394-05-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H7N3O2/c1-3-2-8-4(5(7)10)6(11)9-3/h2H,1H3,(H2,7,10)(H,9,11)

88394-05-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methyl-2-oxo-1H-pyrazine-3-carboxamide

1.2 Other means of identification

Product number -
Other names 5-Methyl-3-oxo-3,4-dihydro-pyrazin-2-carbonsaeure-amid

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:88394-05-2 SDS

88394-05-2Relevant articles and documents

Preparation method, product and application of 2-amino-5-methylpyrazine

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Paragraph 0037-0039; 0048-0050; 0059-0061, (2020/11/25)

The invention belongs to the field of chemical synthesis, and relates to a preparation method, product and application of 2-amino-5-methylpyrazine. The preparation method comprises the following steps: reacting 2-aminomalonamide with pyruvic aldehyde to generate 2-methyl-5-hydroxy-4-pyrazinamide; enabling 2-methyl-5-hydroxy-4-pyrazinamide to react with phosphorus oxychloride so as to generate 2-methyl-5-chloro-4-cyanopyrazine; carrying out a hydrogenation reaction on the 2-methyl-5-chloro-4-cyanopyrazine to generate 2-methyl-4-cyanopyrazine, and hydrolyzing the 2-methyl-4-cyanopyrazine to obtain 2-methyl-4-amide pyrazine; and carrying out Hofmann degradation on the 2-methyl-4-amide pyrazine so as to obtain the 2-methyl-5-aminopyrazine. The method belongs to a brand-new 2-amino-5-methylpyrazine preparation method, is simple and convenient to operate, high in yield and low in cost, and is suitable for industrial large-scale production.

BICYCLIC COMPOUNDS AS ALLOSTERIC SHP2 INHIBITORS

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Paragraph 00681, (2018/08/20)

The present disclosure is directed to inhibitors of SHP2 and their use in the treatment of disease. Also disclosed are pharmaceutical compositions comprising the same.

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