42754-82-5

Usage

Uses

Used in Pharmaceutical Industry:
1H-Pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione, 3-phenylis used as a potential anti-cancer agent for its potential therapeutic benefits in the treatment of various cancers. Its unique structure and properties make it a valuable candidate for further investigation and research in the field of medicinal chemistry, with the aim of developing new and effective cancer treatments.

InChI:InChI=1S/C11H8N4O2/c16-10-7-8(6-4-2-1-3-5-6)14-15-9(7)12-11(17)13-10/h1-5H,(H3,12,13,14,15,16,17)

Upstream product

• 1572-11-8 5-amino-3-phenyl-1H-pyrazole-4-carboxylic acid ethyl ester 
• 57-13-6 urea 
• 129852-43-3 4,6-Bis(methylthio)-3-phenylpyrazolo<3,4-d>pyrimidine 
• 42754-61-0 5-amino-3-phenyl-1H-pyrazole-4-carbonitrile 
• 31646-28-3 4-((methylthio)(phenyl)methylene) morpholinium iodide 
• 111509-91-2 (α-morpholinobenzylidene)malononitrile 
• 2032-36-2 Thiobenzmorpholid 

Relevant academic research and scientific papers

Synthesis of some new pyrazole and pyrazolopyrimidine derivatives [1]

A series of pyrazolo [3,4-d] pyrimidine, pyrazolo [1,5-a] pyrimidine, and pyrazolyl triazoles have been prepared via reaction of ethyl 5-amino-3-phenylpyrazole-4-carboxylate with isothiocyanic esters, α,β-unsaturated nitriles, and some active methylene re

Polarized Ethylenes. IV. Synthesis of Polarized Ethylenes Using Thioamides and Methyl Dithiocarboxylates and their Application to Syntheses of Pyrazoles, Pyrimidines, Pyrazolopyrimidines, and 5-Azacyclazines

Polarized ethylenes having both electron-donating (an amino or a methylthio group) and electron-accepting (cyano, carbamoyl, methyl ester) groups on the adjacent two olefinic carbon atoms were prepared by the condensation of S-alkylthioamidinium salts or