1524-21-6

Basic information

• Product Name: 1-Triazene, 1,3-bis(4-fluorophenyl)-
• CAS NO: 1524-21-6
• Molecular Formula: C12H9F2N3
• Molecular Weight: 233.22
• Mol File: 1524-21-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-Triazene, 1,3-bis(4-fluorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Triazene, 1,3-bis(4-fluorophenyl)-(1524-21-6)
• EPA Substance Registry System: 1-Triazene, 1,3-bis(4-fluorophenyl)-(1524-21-6)

Safety Data

• Hazardous Substances Data: 1524-21-6(Hazardous Substances Data)

Usage

Organic compound

Triazenes 1,3-bis(4-fluorophenyl)-1-triazene is classified as an organic compound, which is a type of chemical compound containing carbon atoms.

Heterocyclic structure

Six-membered ring with three nitrogen atoms The triazene group in this compound consists of a six-membered heterocyclic ring with three nitrogen atoms, making it distinct from other organic compounds.

Presence of a double bond

One double bond in the structure The triazene group also contains a double bond, which contributes to the compound's chemical reactivity and properties.

Application in dyes and pigments

Production use 1,3-bis(4-fluorophenyl)-1-triazene is utilized in the production of dyes and pigments due to its chemical properties, which can impart color to various materials.

Pharmaceutical industry use

Potential medicinal properties This compound is also used in the pharmaceutical industry because of its potential medicinal properties, which may be beneficial in the development of new drugs.

Precautionary measures

Harmful if not properly managed It is crucial to handle and use 1,3-bis(4-fluorophenyl)-1-triazene with caution, as it may pose health risks or cause harm if not managed correctly.

Upstream product

• 371-40-4 4-fluoroaniline 
• 2146-07-8 p-fluoroaniline hydrochloride 

Downstream Products

• 161648-44-8 [Pd₂Cl₂(FC₆H₄NNNC₆H₄F)2(P(CH₂CH₂CH₂CH₃)3)2] 
• 161648-48-2 [Pt₂Cl₂(FC₆H₄NNNC₆H₄F)2(P(CH₂CH₂CH₂CH₃)3)2] 
• 462-06-6 fluorobenzene 
• 81329-32-0 1-(4-fluorophenyl)-1H-pyrazole 
• 371-40-4 4-fluoroaniline 
• 66540-46-3 Rh(CO)(P(C₆H₅)3)2((FC₆H₄)2N₃H)⁽¹⁺⁾*BF₄^(1-)=[Rh(CO)(P(C₆H₅)3)2((FC₆H₄)2N₃H)][BF₄] 
• 800370-15-4 [RhCl(CO)2(p-FC₆H₄NNNHC₆H₄F-p)] 
• 709039-92-9 bis(triethylphosphine)(o-tolyl)(N,N-bis(p-fluorophenyl)triazenido)palladium(II) 
• 267884-39-9 trans-bis(triethylphosphino)(o-tolyl)(N,N'-di-p-fluorophenyltriazenido)nickel(II) 
• 36085-75-3 [Rh2(CO)4(μ-p-FC6H4NNNC6H4F-p)2] 

Relevant articles and documents

Antagonistic Effect of Acetates in C–N Bond Formation with In Situ Generated Diazonium Salts: A Combined Theoretical and Experimental Study

The mechanism of the copper-catalyzed arylation of nitrogen heterocycles using anilines via diazonium salts has been studied by combining DFT and experimental data. A CuI/CuIIIredox mechanism is proposed. Our study has revealed the multiple roles of the acid/base couple AcOH/AcO–. An in situ formed triazene species maintains a low concentration of diazonium salts in the reaction medium, which ensures limited formation of decomposition products. The results of DFT calculations have explained the lower reactivity of imidazole nucleophiles as compared with pyrazole in the arylation reaction.