4706-43-8

Basic information

• Product Name: 1-BENZYL-1H-BENZOTRIAZOLE
• Synonyms: 1-BENZYL-1H-BENZOTRIAZOLE;1-Benzyl-1H-benzo[d][1,2,3]triazole;1-benzylbenzotriazole
• CAS NO: 4706-43-8
• Molecular Formula: C₁₃H₁₁N₃
• Molecular Weight: 209.24654
• Mol File: 4706-43-8.mol
• Article Data: 59

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 1-BENZYL-1H-BENZOTRIAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-BENZYL-1H-BENZOTRIAZOLE(4706-43-8)
• EPA Substance Registry System: 1-BENZYL-1H-BENZOTRIAZOLE(4706-43-8)

Safety Data

• Hazardous Substances Data: 4706-43-8(Hazardous Substances Data)

Usage

General Description

1-Benzyl-1H-benzotriazole is a chemical compound commonly used as a corrosion inhibitor and UV-absorber in various industrial applications. It is a benzotriazole derivative with a benzyl group attached to the nitrogen atom. This chemical is known for its ability to protect metals from corrosion by forming a protective film on the metal surface. Additionally, it has UV-absorbing properties that make it useful in the production of plastics, coatings, and other materials that need protection from the harmful effects of ultraviolet radiation. 1-Benzyl-1H-benzotriazole is considered to be relatively non-toxic and has low environmental impact, making it a popular choice in industrial and commercial settings.

Upstream product

• 95-14-7 1,2,3-Benzotriazole 
• 100-39-0 benzyl bromide 
• 100-44-7 benzyl chloride 
• 54187-96-1 1-(chloromethyl)-1H-benzotriazole 
• 100-58-3 phenylmagnesium bromide 
• 71-43-2 benzene 
• 43183-36-4 1-(trimethylsilyl)-1H-benzotriazole 
• 108-86-1 bromobenzene 
• 28918-29-8 1-((1H-benzotriazol-1-yl)methyl)naphthalen-2-ol 
• 622-79-7 benzyl azide 
• 129112-26-1 2-iodophenyltrifluoromethanesulfonic acid 
• 260783-80-0 N,N,N--trimethyl--1--phenylmethanaminium trifluoromethanesulfonate 
• 28925-45-3 S-methyl O-benzyl dithiocarbonate 
• 6085-94-5 1-benzyl-1,2,4-triazole 

Downstream Products

• 23275-77-6 1-(1-phenylethyl)-1H-benzo[d][1,2,3]triazole 
• 229-87-8 phenanthridine 
• 147861-19-6 2-(1H-1,2,3-benzotriazol-1-yl)-1,2-diphenylethanone 
• 127236-92-4 1,3-dibenzyl-1H-1,2,3-benzotriazol-3-ium bromide 
• 13667-12-4 1-bromo-4-phenylethynylbenzene 
• 142819-61-2 1-(benzotriazol-1-yl)-1,2-diphenylethylene 
• 501-65-5 diphenyl acetylene 
• 198216-25-0 1-Benzotriazol-1-yl-1-phenyl-nonan-2-one 

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.

Synthesis, characterization, and antimicrobial activity of lipophilic N,N′-bis-substituted triazolium salts

A series of N,N′-bis-substituted triazolium salts have been synthesized using 1H-1,2,4-triazole, 1H-1,2,3-triazole, and 1H-1,2,3-benzotriazole. Synthesized compounds were tested for their antimicrobial activities against a panel of representative ESKAPE p

Facile one-pot synthesis of diarylacetylenes from arylaldehydes: Via an addition-double elimination process

A practical one-pot protocol has been developed to synthesize diarylacetylenes from arylaldehydes by treatment with 1-(arylmethyl)benzotriazoles and LiN(SiMe3)2. The reaction proceeded through imine formation, Mannich-type addition and double elimination to deliver products in up to 99% yields with broad substrate scope. In addition, gram-scale synthesis of 1-bromo-4-(phenylethynyl)benzene has been demonstrated.