132980-39-3

Basic information

• Product Name: 4-((1H-benzo[d][1,2,3]triazol-1-yl)methyl)-2,6-di-tert-butylphenol
• Synonyms: 4-((1H-benzo[d][1,2,3]triazol-1-yl)methyl)-2,6-di-tert-butylphenol
• CAS NO: 132980-39-3
• Molecular Weight: 337.465
• Mol File: 132980-39-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-((1H-benzo[d][1,2,3]triazol-1-yl)methyl)-2,6-di-tert-butylphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-((1H-benzo[d][1,2,3]triazol-1-yl)methyl)-2,6-di-tert-butylphenol(132980-39-3)
• EPA Substance Registry System: 4-((1H-benzo[d][1,2,3]triazol-1-yl)methyl)-2,6-di-tert-butylphenol(132980-39-3)

Safety Data

• Hazardous Substances Data: 132980-39-3(Hazardous Substances Data)

Upstream product

• 95-14-7 1,2,3-Benzotriazole 
• 50-00-0 formaldehyd 
• 128-39-2 2,6-di-tert-butylphenol 
• 128-37-0 2,6-di-tert-butyl-4-methyl-phenol 
• 28539-02-8 1-Hydroxymethyl-1H-benzotriazole 

Relevant articles and documents

Electro-oxidative C(sp3)-H Amination of Azoles via Intermolecular Oxidative C(sp3)-H/N-H Cross-Coupling

A method for electrooxidative C(sp3)-H amination via intermolecular oxidative C(sp3)-H/N-H cross-coupling has been developed under metal- and oxidant-free conditions. The C(sp3)-H bonds adjacent to oxygen, nitrogen, and sulfur atoms could all react smoothly with various amines to give the corresponding products with moderate to good yields (30-93%). In addition, the C(sp3)-H bonds of benzylic and allylic are also tolerated in this reaction. A preliminary mechanistic study indicates that the C-H cleavage of tetrahydrofuran is probably not involved in the rate-determining step.

Metal-free cross-dehydrogenative C–N coupling of azoles with xanthenes and related activated arylmethylenes

A metal-free C(sp3)–H/N–H cross-coupling of azoles with xanthenes and related activated arylmethylenes is presented. Both the use of azoles and the activation pattern of C(sp3)–H sources are essential for this transformation. In the