6289-02-7

Basic information

• Product Name: 1-phenyl-1H-pyrazolo[3,4-d]pyrimidine-4,6(2H,5H)-dithione
• CAS NO: 6289-02-7
• Molecular Formula: C₁₁H₈N₄S₂
• Molecular Weight: 260.338
• Mol File: 6289-02-7.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 403.4°C at 760 mmHg
• Flash Point: 197.8°C
• Density: 1.56g/cm³
• Vapor Pressure: 1.02E-06mmHg at 25°C
• Refractive Index: 1.833
• CAS DataBase Reference: 1-phenyl-1H-pyrazolo[3,4-d]pyrimidine-4,6(2H,5H)-dithione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenyl-1H-pyrazolo[3,4-d]pyrimidine-4,6(2H,5H)-dithione(6289-02-7)
• EPA Substance Registry System: 1-phenyl-1H-pyrazolo[3,4-d]pyrimidine-4,6(2H,5H)-dithione(6289-02-7)

Safety Data

• Hazardous Substances Data: 6289-02-7(Hazardous Substances Data)

Usage

Heterocyclic compound

The molecule contains a pyrazolopyrimidine core structure, which is a combination of a pyrazole ring and a pyrimidine ring, both of which contain both carbon and nitrogen atoms.

Pyrazolopyrimidine core structure

The core structure of this compound is formed by the fusion of a pyrazole ring (a five-membered ring with three nitrogen atoms) and a pyrimidine ring (a six-membered ring with four nitrogen atoms).

Two sulfur atoms

This compound contains two sulfur atoms, which are covalently bonded to the pyrazolopyrimidine core structure.

Potential biological and pharmacological activities

1-phenyl-1H-pyrazolo[3,4-d]pyrimidine-4,6(2H,5H)-dithione may exhibit biological or pharmacological properties, making it a potential candidate for further research and development in the field of medicine or drug design.

Building block or intermediate in synthesis

This compound can be used as a starting material or intermediate in the synthesis of other organic compounds, allowing for the creation of more complex molecules with various applications.

Hazardous properties

Due to its chemical composition and potential reactivity, 1-phenyl-1H-pyrazolo[3,4-d]pyrimidine-4,6(2H,5H)-dithione may possess hazardous properties and should be handled with caution.

Controlled laboratory setting

To ensure safety and proper handling, this compound should be used in a controlled laboratory environment, equipped with appropriate safety measures and equipment.

Trained professionals

Only trained professionals with knowledge and experience in handling chemical compounds should work with 1-phenyl-1H-pyrazolo[3,4-d]pyrimidine-4,6(2H,5H)-dithione to minimize the risk of accidents or exposure to hazardous materials.

Upstream product

• 75-15-0 carbon disulfide 
• 5334-43-0 5-Amino-4-cyano-1-phenylpyrazole 
• 100-63-0 phenylhydrazine 

Downstream Products

• 159256-61-8 6-α-carbamoylpropylthio-4-mercapto-1-phenylpyrazolo[3,4-d]pyrimidine 
• 175659-55-9 2-(4-Mercapto-1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-6-ylsulfanyl)-hexanoic acid amide 
• 181702-34-1 2-(4-Mercapto-1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-6-ylsulfanyl)-pentanoic acid amide 
• 181702-33-0 2-(4-Mercapto-1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-6-ylsulfanyl)-3-methyl-butyramide 
• 1298095-84-7 2-(4-Methoxyphenyl)-7-phenyl-2-thioxo-1,2,3,7-tetrahydropyrazolo[3,4-d][1,3,2]diazaphosphinine-4-thione 
• 159256-60-7 4,6-bis-α-carbamoylpropylthio-1-phenylpyrazolo[3,4-d]pyrimidine 
• 134896-39-2 α-(4-methylthio-1-phenylpyrazolo<3,4-d>pyrimidin-6-ylthio)propionamide 
• 134896-40-5 α-(4-amino-1-phenylpyrazolo<3,4-d>pyrimidin-6-ylthio)propionamide 
• 175659-54-8 2-(4-Methylsulfanyl-1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-6-ylsulfanyl)-hexanoic acid amide 
• 181702-37-4 2-(4-Methylsulfanyl-1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-6-ylsulfanyl)-pentanoic acid amide 
• 181702-36-3 3-Methyl-2-(4-methylsulfanyl-1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-6-ylsulfanyl)-butyramide 
• 181702-35-2 2-(4-Methylsulfanyl-1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-6-ylsulfanyl)-butyramide 
• 188727-37-9 12'-(4-methylthio-1-phenylpyrazolo[3,4-d]pyrimidin-6-ylthio)-N-ethyl-dodecanamide 
• 188727-36-8 12'-(4-methylthio-1-phenylpyrazolo[3,4-d]pyrimidin-6-ylthio)dodecanamide 

Relevant articles and documents

Synthesis of new pyrazolopyrimidinedithiones and pyrazolopyrimidinephosphines from aminocyanopyrazoles

A general, high-yielding synthetic protocol for the expedited synthesis of functionalized pyrazolopyrimidine dithione 2 and pyrazolodiazaphosphininethione 3 from amino-cyano pyrazole 1 precursors is presented.