68380-53-0

Basic information

• Product Name: N,1-diphenyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine
• Synonyms: 1H-Pyrazolo[3,4-d]pyrimidin-4-amine, N,1-diphenyl-; N,1-Diphenyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine
• CAS NO: 68380-53-0
• Molecular Formula: C₁₇H₁₃N₅
• Molecular Weight: 287.3186
• Mol File: 68380-53-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 450.2°C at 760 mmHg
• Flash Point: 226.1°C
• Density: 1.29g/cm³
• Vapor Pressure: 2.68E-08mmHg at 25°C
• Refractive Index: 1.711
• CAS DataBase Reference: N,1-diphenyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N,1-diphenyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine(68380-53-0)
• EPA Substance Registry System: N,1-diphenyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine(68380-53-0)

Safety Data

• Hazardous Substances Data: 68380-53-0(Hazardous Substances Data)

Usage

General Description

N,1-diphenyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine is a chemical compound with the molecular formula C18H14N6. It is a pyrazolo[3,4-d]pyrimidine derivative, and it contains a phenyl group and an amine group. This chemical has the potential to exhibit various biological activities due to its structural characteristics, such as its ability to interact with biological targets.

Upstream product

• 5334-48-5 4-chloro-1-(phenyl)-1H-pyrazolo[3,4-d]pyrimidine 
• 62-53-3 aniline 
• 21314-17-0 1-phenyl-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one 
• 16078-71-0 ethyl 5-amino-1-phenyl-1H-pyrazole-4-carboxylate 

Relevant articles and documents

Design, synthesis & evaluation of condensed 2H-4-arylaminopyrimidines as novel antifungal agents

A small, focussed library of condensed 2H-4-arylaminopyrimidines, with 3-diversity points, based on an initial design by molecular docking study of this scaffold at the active site of the fungal enzyme of cytochrome P 450 family, lanosterol 14α

The one-pot conversion of pyrimidinone derivatives into substituted pyrimidines using diphenylphosphinic chloride under a mild condition

Pyrimidinone derivatives reacted with diphenylphosphinic chloride followed by addition of nucleophiles to afford substituted pyrimidine derivatives at a mild temperature (20-66°C).