70380-30-2

Basic information

• Product Name: 1-benzyl-4-(bromomethyl)-1H-1,2,3-triazole
• CAS NO: 70380-30-2
• Molecular Formula: C₁₀H₁₀BrN₃
• Molecular Weight: 252.1105
• Mol File: 70380-30-2.mol
• Article Data: 22

Chemical Properties

• Boiling Point: 389.2°C at 760 mmHg
• Flash Point: 189.2°C
• Density: 1.48g/cm³
• Vapor Pressure: 2.9E-06mmHg at 25°C
• Refractive Index: 1.642
• CAS DataBase Reference: 1-benzyl-4-(bromomethyl)-1H-1,2,3-triazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-benzyl-4-(bromomethyl)-1H-1,2,3-triazole(70380-30-2)
• EPA Substance Registry System: 1-benzyl-4-(bromomethyl)-1H-1,2,3-triazole(70380-30-2)

Safety Data

• Hazardous Substances Data: 70380-30-2(Hazardous Substances Data)

Usage

General Description

1-benzyl-4-(bromomethyl)-1H-1,2,3-triazole is a chemical compound with the molecular formula C9H9BrN3. It is a triazole derivative that contains a benzyl group and a bromomethyl substituent. Triazoles are heterocyclic compounds with a ring structure containing three nitrogen atoms and are widely used in medicinal and agricultural applications. The bromomethyl group in 1-benzyl-4-(bromomethyl)-1H-1,2,3-triazole makes it suitable for further chemical modifications and reactions, and it has potential utility in organic synthesis as a building block for various organic compounds. 1-benzyl-4-(bromomethyl)-1H-1,2,3-triazole may also have biological activity and could be used in the development of pharmaceuticals or other bioactive agents.

Upstream product

• 100-44-7 benzyl chloride 
• 622-79-7 benzyl azide 
• 106-96-7 propargyl bromide 
• 100-39-0 benzyl bromide 
• 28798-81-4 (1-benzyl-[1,2,3]triazol-4-yl)methanol 

Downstream Products

• 27808-16-8 4-methyl-1H-(1,2,3)-triazole 
• 1442449-79-7 C₁₆H₂₅N₅ 
• 1472651-87-8 4-(azidomethyl)-1-benzyl-1H-1,2,3-triazole 
• 1472651-91-4 1-[(1-benzyl-1H-1,2,3-triazol-4-yl)methyl]-4-butyl-5-iodo-1H-1,2,3-triazole 
• 1639236-83-1 C₂₀H₂₁N₃O₄ 
• 1639236-88-6 C₂₀H₂₁N₃O₃ 
• 1639236-90-0 C₂₁H₂₁N₃O₃ 

Relevant articles and documents

Copper(ii) complexes ofN-propargyl cyclam ligands reveal a range of coordination modes and colours, and unexpected reactivity

The coordination chemistry ofN-functionalised cyclam ligands has a rich history, yet cyclam derivatives with pendant alkynes are largely unexplored. This is despite the significant potential and burgeoning application ofN-propargyl cyclams and related com

Catalytic performance of Cu(II)-supported graphene quantum dots modified NiFe2O4 as a proficient nano-catalyst in the synthesis of 1,2,3-triazoles

Abstract: NiFe2O4 nanoparticles are modified by graphene quantum dots (GQDs) and utilized to stabilize the Cu(II) nanoparticles as a novel magnetically retrievable catalytic system (Cu(II)/GQDs/NiFe2O4) for gree

Synthesis, characterization, and investigation of catalytic activity of copper(II) porphyrin graphene oxide for azide–alkyne cycloaddition

Abstract: A covalently cross-linked graphene oxide (GO) catalyst was prepared by a cross-linking process using nucleophilic reaction of copper(II)‐coordinated 5,10,15,20-tetrakis(aminophenyl)porphyrin (CuPPh) with carboxyl groups at the edges of GO (GO–CuPPh). The structure of the catalyst was characterized using different techniques such as Fourier-transform infrared (FT-IR) spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive x-ray spectroscopy (EDS), thermogravimetric analysis (TGA), and inductively coupled plasma (ICP) spectroscopy. All analyses confirmed successful covalent immobilization of CuPPh on GO. The activity of the catalyst was then studied for synthesis of 1,4-disubstituted 1,2,3-triazoles derivatives by reaction of various aryl azides and different terminal alkynes in mild reaction condition with good to excellent yield. Graphical abstract: [Figure not available: see fulltext.].