21717-29-3

Basic information

• Product Name: 2-AMINO-6-ETHYLPYRIDINE
• Synonyms: 6-ETHYLPYRIDIN-2-AMINE;2-AMINO-6-ETHYLPYRIDINE;6-ETHYL-2-PYRIDINAMINE
• CAS NO: 21717-29-3
• Molecular Formula: C₇H₁₀N₂
• Molecular Weight: 122.17
• EINECS: 244-540-7
• Mol File: 21717-29-3.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 218.8 °C at 760 mmHg
• Flash Point: 108.5 °C
• Appearance: /
• Density: 1.037 g/cm³
• Vapor Pressure: 0.124mmHg at 25°C
• Refractive Index: 1.5680
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: 6.98±0.24(Predicted)
• Water Solubility: Slightly soluble in water.
• CAS DataBase Reference: 2-AMINO-6-ETHYLPYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMINO-6-ETHYLPYRIDINE(21717-29-3)
• EPA Substance Registry System: 2-AMINO-6-ETHYLPYRIDINE(21717-29-3)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 36/37/38-22
• Safety Statements: 26-36/37/39
• RIDADR: UN2810
• HazardClass: 6.1
• PackingGroup: III
• Hazardous Substances Data: 21717-29-3(Hazardous Substances Data)

Usage

Uses

The action of iodine on 2-amino-6-ethylpyridine in an alkaline medium gives 2-amino-5-iodo-6-ethylpyridine.

InChI:InChI=1/C7H10N2/c1-2-6-4-3-5-7(8)9-6/h3-5H,2H2,1H3,(H2,8,9)

Upstream product

• 100-71-0 2-Ethylpyridine 
• 95337-73-8 2-(2,5-dimethyl-1H-pyrrol-1-yl)-6-methylpyridine 
• 45644-21-1 6-chloropyridin-2-amine 
• 557-20-0 diethylzinc 
• 32570-89-1 2-(2,5-dimethyl-1H-pyrrol-1-yl)-6-methylpyridine 
• 74-88-4 methyl iodide 

Downstream Products

• 83004-13-1 2‐bromo‐6‐ethylpyridine 
• 906069-78-1 2-[1-(6-ethyl-pyridin-2-ylcarbamoyl)-cyclopentylmethyl]-pentanoic acid benzyl ester 
• 127682-73-9 C₁₆H₁₈N₄O₃S 
• 533939-02-5 N-(6-ethyl-pyridin-2-yl)-2,2-dimethyl-propionamide 
• 939969-11-6 phenyl (6-ethylpyridin-2-yl)carbamate 
• 106592-26-1 N-acetyl-sulfanilic acid-[(6-ethyl-[2]pyridyl)-hydroxy-amide] 
• 108850-70-0 N-acetyl-sulfanilic acid-(6-ethyl-1-oxy-[2]pyridylamide) 
• 109341-45-9 sulfanilic acid-(6-ethyl-1-oxy-[2]pyridylamide) 
• 59146-66-6 6-ethyl-2-cyanopyridine 
• 859788-55-9 3-(2-ethoxy-benzoylamino)-5-ethyl-imidazo[1,2-a]pyridine-2-carboxylic acid amide 
• 859788-87-7 3-(2-ethoxy-phenyl)-5-ethyl-2H-2,4,4b,9-tetraaza-fluoren-1-one 
• 797818-00-9 N,N',N''-tris(6-ethylpyridin-2-yl)benzene-1,3,5-tricarbonamide 
• 686290-03-9 N-(6-ethyl-2-pyridyl)benzamide 
• 477878-37-8 2-[[(6-ethylpyridin-2-yl)imino]methyl]-phenol 

Relevant articles and documents

IMIDAZOPYRIDINES SYK INHIBITORS

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

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

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.