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2-Amino-6-methylpyrazine is an organic compound with the molecular formula C5H6N2. It is a heterocyclic compound featuring a pyrazine ring with an amino group at the 2nd position and a methyl group at the 6th position. 2-Amino-6-methylpyrazine is known for its potential applications in various industries due to its unique chemical properties.

5521-56-2

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5521-56-2 Usage

Uses

Used in Pharmaceutical Industry:
2-Amino-6-methylpyrazine is used as a building block for the synthesis of heterocyclic amides containing pyridyl sulfones. These compounds act as TYK-2 signaling inhibitors, which are beneficial in the treatment of inflammatory and autoimmune diseases. By inhibiting the TYK-2 enzyme, these heterocyclic amides can help regulate immune responses and reduce inflammation, providing therapeutic effects for patients suffering from such conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 5521-56-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,2 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5521-56:
(6*5)+(5*5)+(4*2)+(3*1)+(2*5)+(1*6)=82
82 % 10 = 2
So 5521-56-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H7N3/c1-4-2-7-3-5(6)8-4/h2-3H,1H3,(H2,6,8)

5521-56-2 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (H63436)  2-Amino-6-methylpyrazine, 97%   

  • 5521-56-2

  • 250mg

  • 1000.0CNY

  • Detail
  • Alfa Aesar

  • (H63436)  2-Amino-6-methylpyrazine, 97%   

  • 5521-56-2

  • 1g

  • 3009.0CNY

  • Detail

5521-56-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Methylpyrazin-2-amine

1.2 Other means of identification

Product number -
Other names 6-methylpyrazin-2-amine

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:5521-56-2 SDS

5521-56-2Relevant academic research and scientific papers

ANTIDIABETIC BICYCLIC COMPOUNDS

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Page/Page column 59, (2019/06/09)

Novel compounds of the structural formula (I), and the pharmaceutically acceptable salts thereof, are agonists of G-protein coupled receptor 40 (GPR40) and may be useful in the treatment, prevention and suppression of diseases mediated by the G-protein-co

SYK INHIBITORS

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Paragraph 0279, (2016/02/26)

The present disclosure relates to compounds that are Syk inhibitors and to their use in the treatment of various disease slates, including cancer and inflammatory conditions. In particular embodiments, the structure of the compounds is given by Formula I: wherein R1, R2, R3, and R4 are as described herein. The present disclosure further provides pharmaceutical compositions that include a compound of Formula I, or pharmaceutically acceptable salts thereof, and methods of using these compounds and compositions to treat conditions mediated by Syk. In certain embodiments, also disclosed are methods for treating a cancer in a subject (e.g., a human) in need thereof, comprising administering to the subject a therapeutically effective amount of a compound of formula I, or a pharmaceutically acceptable salt thereof, in combination with a vinca-alkaloid, or a pharmaceutically acceptable salt thereof.

TREATMENT OF CHRONIC GRAFT VERSUS HOST DISEASE WITH SYK INHIBITORS

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Page/Page column 32-33, (2016/11/17)

The present disclosure provides methods of utilizing Syk inhibiting compounds in the treatment for graft versus host disease (GVHD) in a human, including acute graft versus host disease (aGVHD) and chronic graft versus host disease (cGVHD), including the use of compounds selected from the group consisting of the formulas below: (I) and (II).

SYK INHIBITORS

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Paragraph 0242; 0243, (2015/07/02)

The present disclosure relates to compounds that are Syk inhibitors and to their use in the treatment of various disease states, including cancer and inflammatory conditions. In particular embodiments, the structure of the compounds is given by Formula I: wherein R1, R2, R3, and R4 are as described herein. The present disclosure further provides pharmaceutical compositions that include a compound of Formula I, or pharmaceutically acceptable salts or co-crystals thereof, and methods of using these compounds and compositions to treat conditions mediated by Syk.

SYK INHIBITORS

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Page/Page column 99, (2015/07/15)

The present disclosure relates to compounds that are Syk inhibitors and to their use in the treatment of various disease states, including cancer and inflammatory conditions. In particular embodiments, the structure of the compounds is given by Formula I: wherein R1, R2, R3, and R4 are as described herein. The present disclosure further provides pharmaceutical compositions that include a compound of Formula I, or pharmaceutically acceptable salts or co-crystals thereof, and methods of using these compounds and compositions to treat conditions mediated by Syk.

Novel Heterocyclic Compounds and Uses Thereof

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Paragraph 0390, (2013/08/28)

New substituted heterocyclic compounds, compositions containing them, and methods of using them for the inhibition of Raf kinase activity are provided. The new compounds and compositions may be used either alone or in combination with at least one additional agent for the treatment of a Raf kinase mediated disorder, such as cancer.

TRIAZOLE AMIDE DERIVATIVES FOR USE IN THERAPY

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Page/Page column 25-26, (2009/10/22)

The invention relates to triazole amide derivatives of formula (I) for use in therapy, in particular for treating diseases and conditions mediated by antagonism of the mGluR5 receptor, in particular substance related disorders. The invention also relates to certain novel derivatives. In addition, the invention relates to compositions containing the derivatives and processes for their preparation.

NOVEL HETEROCYCLIC COMPOUNDS AND USES THEROF

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Page/Page column 117-118, (2009/10/22)

New substituted heterocyclic compounds, compositions containing them, and methods of using them for the inhibition of Raf kinase activity are provided. The new compounds and compositions may be used either alone or in combination with at least one additional agent for the treatment of a Raf kinase mediated disorder, such as cancer.

A general and efficient route to 6-methyl-pyrazin-2-yl-amines: Alkylation of 2,6-dichloropyrazine via malonate derivatives

Colbon, Paul J. J.,Foster, Alison C.,Giles, Melvyn E.,Patel, Zakariya,Singleton, John T.

experimental part, p. 1451 - 1456 (2009/04/07)

(Chemical Equation Presented) We have developed a convenient two-stage process for the synthesis of 6-methylpyrazine-2-yl-amines from commercially available materials. The procedure involves the synthesis of (6-chloro-pyrazin-2-yl)-acetic acid via arylati

HETEROARYL COMPOUNDS, COMPOSITIONS THEREOF, AND METHODS OF TREATMENT THEREWITH

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Page/Page column 101, (2008/12/05)

Provided herein are Heteroaryl Compounds having the following structure: (I) wherein R1, R2, L, X, Y, Z, Q, A and B are as defined herein, compositions comprising an effective amount of a Heteroaryl Compound and methods for treating or preventing cancer, inflammatory conditions, immunological conditions, metabolic conditions and conditions treatable or preventable by inhibition of a kinase pathway comprising administering an effective amount of a Heteroaryl Compound to a patient in need thereof.

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