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21717-29-3

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21717-29-3 Usage

Description

2-AMINO-6-ETHYLPYRIDINE is an organic compound with the molecular formula C7H10N2. It is a heterocyclic compound, specifically a pyridine derivative, featuring an amino group at the 2nd position and an ethyl group at the 6th position. 2-AMINO-6-ETHYLPYRIDINE is known for its chemical reactivity and potential applications in various industries due to its unique structural properties.

Uses

Used in Pharmaceutical Industry:
2-AMINO-6-ETHYLPYRIDINE is used as an intermediate compound for the synthesis of various pharmaceutical products. Its ability to react with other molecules, such as iodine in an alkaline medium, allows for the creation of new compounds with potential therapeutic applications.
Used in Chemical Synthesis:
2-AMINO-6-ETHYLPYRIDINE serves as a building block in the synthesis of complex organic molecules. Its reactivity with different reagents enables the development of a wide range of chemical products, including those with potential applications in materials science, agrochemicals, and other specialty chemicals.
Used in Research and Development:
As a versatile compound, 2-AMINO-6-ETHYLPYRIDINE is utilized in research and development for exploring new chemical reactions and understanding the properties of related compounds. Its unique structure makes it an interesting subject for studying the effects of various functional groups on the overall chemical behavior of the molecule.

Check Digit Verification of cas no

The CAS Registry Mumber 21717-29-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,7,1 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 21717-29:
(7*2)+(6*1)+(5*7)+(4*1)+(3*7)+(2*2)+(1*9)=93
93 % 10 = 3
So 21717-29-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H10N2/c1-2-6-4-3-5-7(8)9-6/h3-5H,2H2,1H3,(H2,8,9)

21717-29-3 Well-known Company Product Price

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  • Alfa Aesar

  • (A19146)  2-Amino-6-ethylpyridine, 97%   

  • 21717-29-3

  • 2.5g

  • 797.0CNY

  • Detail
  • Alfa Aesar

  • (A19146)  2-Amino-6-ethylpyridine, 97%   

  • 21717-29-3

  • 10g

  • 1473.0CNY

  • Detail
  • Alfa Aesar

  • (A19146)  2-Amino-6-ethylpyridine, 97%   

  • 21717-29-3

  • 50g

  • 6135.0CNY

  • Detail

21717-29-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-ethylpyridin-2-amine

1.2 Other means of identification

Product number -
Other names 2-Pyridinamine,6-ethyl

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:21717-29-3 SDS

21717-29-3Relevant articles and documents

IMIDAZOPYRIDINES SYK INHIBITORS

-

Paragraph 0372, (2014/06/11)

Certain imidazopyridines (I) and pharmaceutical compositions thereof are provided herein. Methods of treating patients suffering from certain diseases and disorders responsive to the inhibition of Syk activity, which comprises administering to such patients an amount of at least one chemical entity effective to reduce signs or symptoms of the disease or disorder are provided. Also provided are methods for determining the presence or absence of Syk kinase in a sample.

ANTI-VIRAL COMPOUNDS

-

Page/Page column 58, (2008/12/08)

Compounds effective in inhibiting replication of Hepatitis C virus ( HCV ) or other viruses are disclosed. This invention is also directed to compositions comprising such compounds, coformulation or co-administration of such compounds with other anti-viral or therapeutic agents, processes and intermediates for the syntheses of such compounds, and methods of using such compounds for the treatment of HCV or other viral infections.

Protection of Primary Amines as N-Substituted 2,5-Dimethylpyrroles

Breukelman, Stephen P.,Meakins, G. Denis,Tirel, Malcolm D.

, p. 800 - 801 (2007/10/02)

Protection of a primary amine group against attack by organic or aqueous solutions of strong bases or nucleophiles is achieved by incorporation into an N-substituted 2,5-dimethylpyrrole system from which the amine group is regenerated by treatment with hydroxylamine hydrochloride.

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