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 
• 100-44-7 benzyl chloride 
• 5822-13-9 N-benzyl-1,2-phenylenediamine 
• 100-39-0 benzyl bromide 
• 54187-96-1 1-(chloromethyl)-1H-benzotriazole 
• 100-58-3 phenylmagnesium bromide 
• 71-43-2 benzene 
• 133349-89-0 1-(1H-Benzotriazol-1-ylmethyl)-2-methoxynaphthalene 
• 133349-87-8 2-(1H-Benzotriazol-1-ylmethyl)-1,3,5-trimethoxybenzene 
• 43183-36-4 1-(trimethylsilyl)-1H-benzotriazole 
• 57710-80-2 1-benzyloxycarbonyl-1Hbenzo[d][1.2.3]triazole 
• 6085-94-5 1-benzyl-1,2,4-triazole 
• 108-86-1 bromobenzene 
• 5729-06-6 N-benzyl-2-nitroaniline 

Downstream Products

• 142087-22-7 1-(1-isopropyl-1-phenylmethyl)benzotriazole 
• 142087-21-6 1-(benzotriazol-1-yl)-1-phenylpentane 
• 142087-23-8 5-(benzotriazol-1-yl)-5-phenylnonane 
• 142819-53-2 1-(benzotriazol-1-yl)-2-tosylamino-1,2-diphenylethane 
• 95-14-7 1,2,3-Benzotriazole 
• 62-53-3 aniline 
• 501-65-5 diphenyl acetylene 
• 142819-61-2 1-(benzotriazol-1-yl)-1,2-diphenylethylene 
• 142819-59-8 2-anilino-1-(benzotriazol-1-yl)-1,2-diphenylethane 
• 142819-57-6 1-(benzotriazol-1-yl)-2-tosylamino-2-(3-thienyl)-1-phenylethane 
• 142087-24-9 2-(benzotriazol-1-yl)-1,2,3-triphenylpropane 
• 54212-63-4 1,2-di(N-methylanilino)-1,2-diphenylethene 
• 7510-33-0 N,N'-diphenyl-1,2-diphenylethane-1,2-diimine 
• 229-87-8 phenanthridine 

Relevant articles and documents

Scalable Synthesis of Benzotriazoles via [3+2] Cycloaddition of Azides and Arynes in Flow

A method for the metal-free synthesis of benzotriazoles in flow is reported. Using azides and in situ generated arynes, benzotriazoles are formed in a [3+2] cycloaddition within minutes. Employing different substitution patterns of the azide and aryne coupling partners, a modular access to benzotriazoles is provided. Thermal strain of hazardous azides and accumulation of reactive intermediates is minimized by short reaction times in flow, improving the safety profile of the process. The scalability of the reaction is demonstrated.

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

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.