1299471-89-8

Basic information

• Product Name: 2-methyl-5-[(E)-2-phenylethenyl]-2H-tetrazole
• Synonyms: 2-methyl-5-[(E)-2-phenylethenyl]-2H-tetrazole
• CAS NO: 1299471-89-8
• Molecular Weight: 186.216
• Mol File: 1299471-89-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-methyl-5-[(E)-2-phenylethenyl]-2H-tetrazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methyl-5-[(E)-2-phenylethenyl]-2H-tetrazole(1299471-89-8)
• EPA Substance Registry System: 2-methyl-5-[(E)-2-phenylethenyl]-2H-tetrazole(1299471-89-8)

Safety Data

• Hazardous Substances Data: 1299471-89-8(Hazardous Substances Data)

Upstream product

• 15284-39-6 2-methyl-5-vinyl-2H-tetrazole 
• 591-50-4 iodobenzene 
• 74-88-4 methyl iodide 
• 108-86-1 bromobenzene 

Downstream Products

• 1442645-30-8 5-(2,2-diphenylethyl)-2-methyl-2H-tetrazole 

Relevant articles and documents

A second-generation ligand for the enantioselective rhodium-catalyzed addition of arylboronic acids to alkenylazaarenes

A 2,4,6-trialkylanilide-containing chiral diene has been identified as a superior ligand for the enantioselective rhodium-catalyzed arylation of alkenylazaarenes with arylboronic acids.

Vinyltetrazoles: III. Metal-catalyzed arylation, a new method of vinyltetrazoles functionalization

New functionalization procedure was developed for C- and N-vinyltetrazoles based on Heck reaction. Applying this method diverse (E)-styryl- and (E)-distyryltetrazoles were obtained for the first time in 76-85% yields. C-Vinyltetrazoles are more reactive in Heck cross-coupling than N-vinyltetrazoles. The arylation of 1-vinyltetrazole along Heck reaction proceeds with a C-H-activation and leads to the formation of 5-phenyl-1-[2-(E)-phenylethenyl]tetrazole.