16462-29-6

Basic information

• Product Name: 4-AMINO-2-ETHYLSULFANYL-PYRIMIDINE-5-CARBONITRILE
• Synonyms: 4-AMINO-2-ETHYLSULFANYL-PYRIMIDINE-5-CARBONITRILE;4-Amino-2-(ethylthio)-5-pyrimidinecarbonitrile;5-Cyano-4-amino-2-ethylsulfanylpyrimidine;5-PyriMidinecarbonitrile,4-aMino-2-(ethylthio)-;4-amino-2-(ethylthio)pyrimidine-5-carbonitrile
• CAS NO: 16462-29-6
• Molecular Formula: C7H8N4S
• Molecular Weight: 180.23022
• Mol File: 16462-29-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 399.013 °C at 760 mmHg
• Flash Point: 195.116 °C
• Appearance: /
• Density: 1.326 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.621
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: 4-AMINO-2-ETHYLSULFANYL-PYRIMIDINE-5-CARBONITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-AMINO-2-ETHYLSULFANYL-PYRIMIDINE-5-CARBONITRILE(16462-29-6)
• EPA Substance Registry System: 4-AMINO-2-ETHYLSULFANYL-PYRIMIDINE-5-CARBONITRILE(16462-29-6)

Safety Data

• Hazardous Substances Data: 16462-29-6(Hazardous Substances Data)

Usage

General Description

4-Amino-2-ethylsulfanyl-pyrimidine-5-carbonitrile is a chemical compound with the molecular formula C7H9N5S. It is a pyrimidine derivative and contains an amino group, an ethylsulfanyl group, and a carbonitrile group. 4-AMINO-2-ETHYLSULFANYL-PYRIMIDINE-5-CARBONITRILE has potential applications in pharmaceutical research and development, particularly in the synthesis of new drugs and pharmaceutical products. Its unique structure and properties make it a valuable building block for the creation of various biologically active compounds. It may also have potential uses in the field of agrochemicals and materials science. Overall, 4-Amino-2-ethylsulfanyl-pyrimidine-5-carbonitrile is a versatile and important chemical with diverse potential applications in various scientific and industrial fields.

InChI:InChI=1/C7H8N4S/c1-2-12-7-10-4-5(3-8)6(9)11-7/h4H,2H2,1H3,(H2,9,10,11)

Upstream product

• 1071-37-0 2-ethylisothiourea hydrobromide 
• 123-06-8 Ethoxymethylenemalononitrile 
• 13882-27-4 ethyl imidothiocarbamate hydroiodide 
• 2986-20-1 S-ethylisothiourea 
• 317830-03-8 4-chloro-2-ethylsulfanylpyrimidine-5-carbonitrile 

Downstream Products

• 16462-28-5 5-cyanocytosine 
• 16462-27-4 2,4-diamino-pyrimidine-5-carbonitrile 
• 1076222-91-7 4-[4-methyl-2-(7-piperidin-1-yl-pyrimido[4,5-d]pyrimidin-4-ylamino)-phenylsulfanyl]-phenol trifluoroacetate 
• 1076222-90-6 4-[2-(7-ethylsulfanyl-pyrimido[4,5-d]pyrimidin-4-ylamino)-4-methyl-phenylsulfanyl]-phenol trifluoroacetate 
• 944504-68-1 C₂₄H₂₄N₆OS 
• 944504-74-9 C₂₃H₂₂N₆O₂S 
• 1365922-48-0 C₂₅H₁₉N₅O₂S 
• 1365922-44-6 C₂₁H₁₉N₅O₂S 
• 1365922-39-9 C₂₀H₁₇N₅O₂S 
• 944504-63-6 C₂₁H₁₉N₅OS₂ 
• 7403-31-8 7-ethylmercapto-3H-pyrimido[4,5-d]pyrimidine-4-thione 
• 4458-18-8 5-(aminomethyl)pyrimidine-2,4-diamine 
• 7403-27-2 7-ethylmercapto-3H-pyrimido[4,5-d]pyrimidin-4-one 
• 98021-40-0 4-amino-2-oxo-1,2-dihydro-pyrimidine-5-carboxylic acid amide 

Relevant articles and documents

Synthesis and anticancer activity of novel 2-alkylthio-4-amino-5-(thiazol-2-YL)pyrimidines

A series of new fist-time synthesized of thiazolyl-substituted 4-aminopyrimidine was obtained on the basis of a two-stage process including thioamidation of 4-amino-5-cyanopyrimide followed by one-pot acylation and Hantzsch synthesis in good yield (52–77%

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.