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5521-56-2

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5521-56-2 Usage

Uses

6-Methylpyrazin-2-amine is used in the preparation of heterocyclic amides containing pyridyl sulfones as TYK-2 signaling inhibitors useful in treatment of inflammatory and autoimmune diseases.

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
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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 articles and documents

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

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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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.

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