38446-59-2

Basic information

• Product Name: 2H-Tetrazole, 5-(4-methoxyphenyl)-2-(4-methylphenyl)-
• CAS NO: 38446-59-2
• Molecular Formula: C15H14N4O
• Molecular Weight: 266.302
• Mol File: 38446-59-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2H-Tetrazole, 5-(4-methoxyphenyl)-2-(4-methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Tetrazole, 5-(4-methoxyphenyl)-2-(4-methylphenyl)-(38446-59-2)
• EPA Substance Registry System: 2H-Tetrazole, 5-(4-methoxyphenyl)-2-(4-methylphenyl)-(38446-59-2)

Safety Data

• Hazardous Substances Data: 38446-59-2(Hazardous Substances Data)

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 50626-26-1 N'-[(E)-(4-methoxyphenyl)methylidene]benzenesulfonylhydrazone 
• 106-49-0 p-toluidine 
• 5720-05-8 4-methylphenylboronic acid 
• 6926-51-8 5-(4-methoxyphenyl)-2H-tetrazole 

Downstream Products

• 21798-24-3 2,3-bis-(4-methoxy-phenyl)-5,6-diphenyl-pyrazine 
• 1694-19-5 p-methoxystilbene 
• 142312-23-0 3-(4-Methoxy-phenyl)-5-phenyl-1-p-tolyl-1H-[1,2,4]triazole 
• 142312-24-1 3,5-Bis-(4-methoxy-phenyl)-1-p-tolyl-1H-[1,2,4]triazole 

Relevant articles and documents

Light-Induced Tetrazole-Quinone 1,3-Dipolar Cycloadditions

Quinones were firstly used as dipolarophiles in a photoclick 1,3-cycloaddition with 2,5-diaryltetrazoles, as photoactivatable predipoles, providing a novel and efficient access to three types of pyrazole-fused quinones (indazoledione derivatives). Distinc

Efficient synthesis of 2,5-disubstituted tetrazoles via the Cu 2O-catalyzed aerobic oxidative direct cross-coupling of N-H free tetrazoles with boronic acids

We present a new protocol that allows for the synthesis of 2,5-disubstituted tetrazoles via the direct coupling of N-H free tetrazoles and low toxic boronic acids in the presence of only a catalytic amount of Cu 2O (5 mol%) as catalyst and 1 atm of environmentally benign O 2 as oxidant, without the need for other additives. This method represents a simple, green, and atom-efficient synthesis of 2,5-disubstituted tetrazoles. The Royal Society of Chemistry 2012.

Palladium- and copper-catalyzed selective arylation of 5-aryltetrazoles by diaryliodonium salts

Palladium(0)-catalyzed arylation of 5-aryltetrazoles in t-BuOH at 80°C with diaryliodonium salts proceeds in the presence of copper(II) phenylcyclopropyl carboxylate regioselectively at the N2 position.