153562-20-0

Basic information

• Product Name: 7-PHENYL-5-(TRIFLUOROMETHYL)[1,2,3,4]TETRAAZOLO[1,5-A]PYRIMIDINE
• Synonyms: 7-PHENYL-5-(TRIFLUOROMETHYL)[1,2,3,4]TETRAAZOLO[1,5-A]PYRIMIDINE;7-phenyl-5-(trifluoromethyl)-[1,2,3,4]tetrazolo[1,5-a]pyrimidine
• CAS NO: 153562-20-0
• Molecular Formula: C11H6F3N5
• Molecular Weight: 265.19
• Mol File: 153562-20-0.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 7-PHENYL-5-(TRIFLUOROMETHYL)[1,2,3,4]TETRAAZOLO[1,5-A]PYRIMIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 7-PHENYL-5-(TRIFLUOROMETHYL)[1,2,3,4]TETRAAZOLO[1,5-A]PYRIMIDINE(153562-20-0)
• EPA Substance Registry System: 7-PHENYL-5-(TRIFLUOROMETHYL)[1,2,3,4]TETRAAZOLO[1,5-A]PYRIMIDINE(153562-20-0)

Safety Data

• Hazardous Substances Data: 153562-20-0(Hazardous Substances Data)

Upstream product

• 4418-61-5 5-aminotetrazole 
• 326-06-7 1-Phenyl-4,4,4-trifluorobutane-1,3-dione 

Relevant articles and documents

Investigation on the reactions of fluorinated 1,3-diketones with 5-aminotetrazole: Synthesis of some tetrazolopyrimidines and β-ketoamine derivatives

Reactions of 5-aminotetrazole (II) with fluorinated 1,3-diketones (Ia-c) in different media have been investigated and found to be solvent dependent.Tetrazolopyrimidines (IIIa-c) are exclusively obtained in gl. acetic acid while β-ketoamines (Va-c) of tetrazole along with IIIa-c are obtained in abs. ethanol.The spectral data of the free schiff bases indicate that the site of amine condensation in unsymmetrical β-ketoamines is the lesser enolized acyl oxygen and the ketoamino-form is the predominant tautometer.The proposed structures are fully corroborated by IR, PMR, 19F NMR and mass spectral data.