36226-16-1

Basic information

• Product Name: 5,7-dimethyl-2-phenyl-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione
• Synonyms: 5,7-dimethyl-2-phenyl-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione
• CAS NO: 36226-16-1
• Molecular Weight: 256.264
• Mol File: 36226-16-1.mol

Chemical Properties

• CAS DataBase Reference: 5,7-dimethyl-2-phenyl-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 5,7-dimethyl-2-phenyl-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione(36226-16-1)
• EPA Substance Registry System: 5,7-dimethyl-2-phenyl-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione(36226-16-1)

Safety Data

• Hazardous Substances Data: 36226-16-1(Hazardous Substances Data)

Upstream product

• 132124-82-4 6-amino-1,3-dimethyl-5-[(phenylimino)methyl]uracil 

Relevant articles and documents

A new synthesis of pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-diones by oxidative N-N bond formation of 6-amino-5-(N-aryliminomethyl)uracils using iodobenzene diacetate

The intramolecular cyclizations of 6-amino-5-(N-aryliminomethyl)-1,3-dimethyluracils (2) involving the N-N bond formation were effected via a hypervalent iodine oxidation using iodobenzene diacetate. This method enabled a facile synthesis of 2-aryl-5,7-di

Iodobenzene diacetate-promoted N-N and N-O bond formation for pyrazolo- and isoxazolopyrimidine syntheses

Pyrazolo[3,4-d]pyrimidine-4,6-dione derivatives were efficiently synthesized via the intramolecular N-N bond coupling of 5-iminomethyl-6-aminouracil derivatives using iodobenzene diacetate. The oxidative coupling was also applied to the analogous N-O bond