833433-13-9

Basic information

• Product Name: methyl 7-(3-fluorophenyl)-5-methyl-4,7-dihydrotetraazolo[1,5-a]pyrimidine-6-carboxylate
• Synonyms: methyl 7-(3-fluorophenyl)-5-methyl-4,7-dihydrotetraazolo[1,5-a]pyrimidine-6-carboxylate
• CAS NO: 833433-13-9
• Molecular Formula: C₁₃H₁₂FN₅O₂
• Molecular Weight: 289.2650832
• Mol File: 833433-13-9.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: methyl 7-(3-fluorophenyl)-5-methyl-4,7-dihydrotetraazolo[1,5-a]pyrimidine-6-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 7-(3-fluorophenyl)-5-methyl-4,7-dihydrotetraazolo[1,5-a]pyrimidine-6-carboxylate(833433-13-9)
• EPA Substance Registry System: methyl 7-(3-fluorophenyl)-5-methyl-4,7-dihydrotetraazolo[1,5-a]pyrimidine-6-carboxylate(833433-13-9)

Safety Data

• Hazardous Substances Data: 833433-13-9(Hazardous Substances Data)

Upstream product

• 4418-61-5 5-aminotetrazole 
• 105-45-3 acetoacetic acid methyl ester 
• 456-48-4 3-Fluorobenzaldehyde 

Relevant articles and documents

A novel magnetically recyclable silver-loaded cellulose-based bionanocomposite catalyst for green synthesis of tetrazolo[1,5-a]pyrimidines

5-Methyl-7-aryl-4,7-dihydrotetrazolo[1,5-a]pyrimidine-6-carboxylic ester derivatives were efficiently synthesized by reaction of methyl or ethyl acetoacetate, 5-aminotetrazole (produced from 2-cyanoguanidine and sodium azide), and various aromatic aldehydes in presence of a new cellulose-based Ag-loaded magnetic bionanostructure. This protocol offers many advantages such as short reaction time, high yield, the remarkable magnetic property of the nanocomposite, and easy separation of the nanocatalyst from the reaction mixture without considerable loss of catalytic activity. Furthermore, X-ray diffraction analysis, field-emission scanning electron microscopy, and energy-dispersive X-ray (EDX) analysis were used to characterize the prepared nanocatalyst.

Solvent-free synthesis of 5-methyl-7-aryl-4,7-dihydrotetrazolo[1,5-a] pyrimidine-6-carboxylic esters catalyzed by sulfamic acid

(Chemical Equation Presented) The solvent-free synthesis of 5-methyl-7-aryl-4,7-dihydrotetrazolo[1,5-a]pyrimidine-6-carboxylic esters was performed and effectively catalyzed by sulfamic acid. Compared with conventional methods, this protocol features mild reaction conditions and high yields. Furthermore, it is solvent-free and thus ecofriendly.