64301-13-9

Basic information

• Product Name: 2-Propanone, 1-[5-methyl-2-[(phenylmethyl)thio][1,2,4]triazolo[1,5-a]pyrimidin-7-yl]-
• CAS NO: 64301-13-9
• Molecular Formula: C16H16N4OS
• Molecular Weight: 312.395
• Mol File: 64301-13-9.mol

Chemical Properties

• CAS DataBase Reference: 2-Propanone, 1-[5-methyl-2-[(phenylmethyl)thio][1,2,4]triazolo[1,5-a]pyrimidin-7-yl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propanone, 1-[5-methyl-2-[(phenylmethyl)thio][1,2,4]triazolo[1,5-a]pyrimidin-7-yl]-(64301-13-9)
• EPA Substance Registry System: 2-Propanone, 1-[5-methyl-2-[(phenylmethyl)thio][1,2,4]triazolo[1,5-a]pyrimidin-7-yl]-(64301-13-9)

Safety Data

• Hazardous Substances Data: 64301-13-9(Hazardous Substances Data)

Upstream product

• 3922-47-2 3-(benzylthio)-1H-1,2,4-triazol-5-amine 

Relevant articles and documents

On triazoles. XXXV. The reaction of 5-amino-1,2,4-triazoles with di- and triketones

The reaction of 5-amino-3-Q-1H-1,2,4-triazoles 1 with aliphatic, aromatic and cyclic 1,3-diketones, 1,4-diketones, and different linear and non linear triketones was studied. It was proved that in case of unsymmetrical aliphatic 1,3-diketones the regiochemical outcome of the reaction was influenced by steric factors. In case of triacetylmethane and 3-(4-chlorobenzyl)-2,4-pontanedione the splitting of one acetyl group from the reactant was observed during the reaction. A liner triketone, namely the 2,4,6-trioxoheptane reacted as a simple 1,3-diketone.

2-SUBSTITUTED-S-TRIAZOLO[1,5A]-PYRIMIDINES

2-Substituted-s-triazolo[1,5a]pyrimidines are disclosed which are useful as inhibitors of phosphodiesterase enzymes or intermediates in the production process. Such comoounds are of the following structure: wherein X, R, R1, R2 and R3 are as defined herei