90476-12-3

Basic information

• Product Name: [(2E)-3-(4-bromophenyl)-1-methyltriaz-2-en-1-yl]methyl acetate
• CAS NO: 90476-12-3
• Molecular Formula: C₁₀H₁₂BrN₃O₂
• Molecular Weight: 286.1252
• Mol File: 90476-12-3.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 339.6°C at 760 mmHg
• Flash Point: 159.2°C
• Density: 1.43g/cm³
• Vapor Pressure: 9.1E-05mmHg at 25°C
• Refractive Index: 1.569
• CAS DataBase Reference: [(2E)-3-(4-bromophenyl)-1-methyltriaz-2-en-1-yl]methyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: [(2E)-3-(4-bromophenyl)-1-methyltriaz-2-en-1-yl]methyl acetate(90476-12-3)
• EPA Substance Registry System: [(2E)-3-(4-bromophenyl)-1-methyltriaz-2-en-1-yl]methyl acetate(90476-12-3)

Safety Data

• Hazardous Substances Data: 90476-12-3(Hazardous Substances Data)

Usage

Description

[(2E)-3-(4-bromophenyl)-1-methyltriaz-2-en-1-yl]methyl acetate is a chemical compound characterized by its molecular formula C12H12BrN3O2. It is a derivative of 4-bromophenyl and triazene, featuring a methyl acetate group attached. [(2E)-3-(4-bromophenyl)-1-methyltriaz-2-en-1-yl]methyl acetate may exhibit unique chemical and biological properties due to the presence of bromophenyl and triazene moieties, making it a candidate for various applications across different industries.

Uses

Used in Pharmaceutical Industry:
[(2E)-3-(4-bromophenyl)-1-methyltriaz-2-en-1-yl]methyl acetate is used as a reagent or substrate for the synthesis of other compounds, potentially contributing to the development of new pharmaceuticals. Its unique structure may allow it to interact with biological targets, making it a valuable component in the creation of novel drugs.
Used in Agricultural Industry:
In agriculture, [(2E)-3-(4-bromophenyl)-1-methyltriaz-2-en-1-yl]methyl acetate may be utilized for the development of new agrochemicals, such as pesticides or herbicides. Its potential biological activities could be harnessed to create more effective and targeted products for crop protection and management.
Used in Chemical Synthesis:
[(2E)-3-(4-bromophenyl)-1-methyltriaz-2-en-1-yl]methyl acetate is used as a building block in the synthesis of various organic compounds. Its unique structure and functional groups make it a versatile component in the creation of complex molecules for a wide range of applications, from materials science to specialty chemicals.

Upstream product

• 106-40-1 4-bromo-aniline 
• 108-24-7 acetic anhydride 
• 73779-15-4 1-p-bromophenyl-3-hydroxymethyl-3-methyltriazene 

Downstream Products

• 90476-21-4 1-p-bromophenyl-3-methyl-3-methoxymethyltriazene 

Relevant articles and documents

OPEN-CHAIN NITROGEN COMPOUNDS. PART V. HYDROXYMETHYLTRIAZENES: SYNTHESIS OF SOME NEW ALKYL HOMOLOGUES OF THE ANTI-TUMOUR 3-METHYL-3-HYDROXYMETHYLTRIAZENES AND PREPARATION OF THE DERIVED ACETOXYMETHYL-, BENZOYLOXYMETHYL-, AND METHOXYMETHYLTRIAZENES

The synthesis of some new 1-aryl-3-alkyl-3-hydroxymethyltriazenes is described.The method of coupling a diazonium salt with an alkylamine/formaldehyde mixture has been extended to (a) some diazonium ions with para substituents other than -M groups, (b) those with substituents in ortho position, and (c) to homologous alkylamines (e.g. ethylamine, propylamine, etc.).Hydroxymethyltriazenes can also be prepared by the reaction of a 1-aryl-3-methyltriazene with formaldehyde.Several new derivatives of hydroxymethyl function have been prepared.Reaction with acetic anhydride or benzoyl chloride in pyridine affords respectively the acetoxymethyl- and benzoyloxymethyl-triazenes; the acetates and benzoates react readily with methanol to give the novel methoxymethyltriazenes.This is the first report of a series of dialkyltriazenes with an ether linkage in the α position. An ether of this type has also been obtained directly from the diazonium fluoroborate salt by coupling with a mixture of benzylamine and formaldehyde in ethanolic solution.