173045-49-3

Basic information

• Product Name: 1-(3-methoxybenzyl)-1H-benzo[d][1,2,3]triazole
• Synonyms: 1-(3-methoxybenzyl)-1H-benzo[d][1,2,3]triazole
• CAS NO: 173045-49-3
• Molecular Weight: 239.277
• Mol File: 173045-49-3.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-(3-methoxybenzyl)-1H-benzo[d][1,2,3]triazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-methoxybenzyl)-1H-benzo[d][1,2,3]triazole(173045-49-3)
• EPA Substance Registry System: 1-(3-methoxybenzyl)-1H-benzo[d][1,2,3]triazole(173045-49-3)

Safety Data

• Hazardous Substances Data: 173045-49-3(Hazardous Substances Data)

Upstream product

• 54187-96-1 1-(chloromethyl)-1H-benzotriazole 
• 2398-37-0 3-methoxyphenyl bromide 
• 95-14-7 1,2,3-Benzotriazole 
• 1334478-53-3 Br^(1-)*C₂₂H₂₂N₃O₂⁽¹⁺⁾ 
• 1262319-57-2 C₂₀H₁₆N₆O 
• 874-98-6 1-bromomethyl-3-methoxybenzene 

Relevant articles and documents

A convenient way for alkylation of amines using xanthate esters

N-alkylation of amines by the reaction with xanthate esters in the presence of acetic acid catalyst in ethanol is reported. Short reaction time, high yield, general applicability and environmentally benign nature are the noteworthy features of our protocol. The probable mechanism for the formation N-alkylation of amines is proposed.

Convenient and stereoselective synthesis of symmetrical (E)-stilbenes via homocoupling of 1,3-dibenzylbenzotriazolium bromides

Using NaH as the base and DMSO as the solvent, a series of symmetric (E)-stilbenes were prepared in good yields via the -homocoupling of 1,3-dibenzylbenzotriazolium bromides at room temperature. Georg Thieme Verlag Stuttgart · New York.

Nucleophilic substitution of benzotriazolylalkyl chlorides with Grignard reagents: A direct route to benzotriazoloalkyl(hetero)aromatic compounds

Benzotriazolylalkyl chlorides 5 react with (hetero)aromatic Grignard reagents generated from the corresponding halogen derivatives to afford benzotriazoloalkyl(hetero)aromatic compounds 8a-k and 10a-c in good yields.