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2-Amino-3-cyano-5-methylpyrazine is a pyrazine derivative with the molecular formula C7H7N5, featuring an amino group, a cyano group, and a methyl group. This chemical compound is known for its potential applications in various industries due to its unique properties.

17890-82-3

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17890-82-3 Usage

Uses

Used in Food Industry:
2-Amino-3-cyano-5-methylpyrazine is used as a flavoring agent for adding a roasted and nutty flavor to various food products, enhancing the taste and aroma of the final product.
Used in Pharmaceutical Production:
2-Amino-3-cyano-5-methylpyrazine is utilized in the production of pharmaceuticals, where its unique chemical structure contributes to the development of new drugs with potential therapeutic benefits.
Used in Agrochemicals:
2-Amino-3-cyano-5-methylpyrazine is also used in the production of agrochemicals, where it may contribute to the development of new pesticides or other agricultural products.
Used in Medicinal Applications:
2-Amino-3-cyano-5-methylpyrazine has been studied for its potential antioxidant and anti-inflammatory properties, making it a promising candidate for various medicinal applications, such as the development of new treatments for inflammatory diseases or conditions related to oxidative stress.
However, it is crucial to handle 2-Amino-3-cyano-5-methylpyrazine with care, as it may have harmful effects if not used properly, highlighting the importance of safety measures in its application across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 17890-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,9 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17890-82:
(7*1)+(6*7)+(5*8)+(4*9)+(3*0)+(2*8)+(1*2)=143
143 % 10 = 3
So 17890-82-3 is a valid CAS Registry Number.

17890-82-3SDS

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 3-amino-6-methylpyrazine-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 3-Amino-6-methyl-pyrazin-2-carbonitril

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:17890-82-3 SDS

17890-82-3Downstream Products

17890-82-3Relevant academic research and scientific papers

Novel 1-(2-aminopyrazin-3-yl)methyl-2-thioureas as potent inhibitors of mitogen-activated protein kinase-activated protein kinase 2 (MK-2)

Lin, Songnian,Lombardo, Matthew,Malkani, Sunita,Hale, Jeffrey J.,Mills, Sander G.,Chapman, Kevin,Thompson, James E.,Zhang, Wen Xiao,Wang, Ruixiu,Cubbon, Rose M.,O'Neill, Edward A.,Luell, Silvi,Carballo-Jane, Ester,Yang, Lihu

scheme or table, p. 3238 - 3242 (2010/05/02)

Novel 1-(2-aminopyrazin-3-yl)methyl-2-thioureas are described as inhibitors of mitogen-activated protein kinase-activated protein kinase 2 (MK-2). These compounds demonstrate potent in vitro activity against the enzyme with IC50 values as low as 15 nM, and suppress expression of TNFα in THP-1 cells and in vivo in an acute inflammation model in mice. The synthesis, structure-activity relationship (SAR), and biological evaluation of these compounds are discussed.

Studies on Pyrazines; Part 20. A Simple Synthesis of 5-Substituted 2-Amino-3-cyanopyrazines: Useful Intermediates for Pteridine Synthesis

Sato, Nobuhiro,Takeuchi, Ryo

, p. 659 - 660 (2007/10/02)

A new and convenient synthesis of 5-substituted 2-amino-3-cyanopyrazines 3 involving cyanation of the corresponding 2-amino-3-bromopyrazines 2 with sodium dicyanocuprate is reported.

Pteridines. 47. Preparation and Chemistry of 2-Amino-6-carbalkoxy-3-cyano-5-substituted Pyrazine 1-Oxides: Synthesis of Pterin-6-carboxaldehyde

Taylor, Edward C.,Dumas, Donald J.

, p. 2485 - 2489 (2007/10/02)

A new procedure for the synthesis of 2-amino-3-cyano-5-substituted pyrazines 9, useful intermediates for the synthesis of pteridines, is described.Oximation of β-keto esters 2 followed by reaction with aminomalononitrile provides 2-amino-6-carbalkoxy-3-cyano-5-substituted pyrazine 1-oxides 5.Protection of the amino group as its ((dimethylamino)methylene)amino derivative 9 followed by SN2 decarbalkoxylation provides pyrazines 10 which on removal of the protecting group and deoxygenation give pyrazines 8.This method is designed to be of use in cases where the β-keto ester cannot be converted directly to the corresponding α-keto aldoxime 3.The procedure is applied to the synthesis of 2-amino-3-cyano-5-(dimethoxymethyl)pyrazine (8a), an intermediate in the synthesis of pterin-6-carboxaldehyde (1).

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