22715-73-7

Basic information

• Product Name: (1E)-1,3-bis(4-methoxyphenyl)triaz-1-ene
• CAS NO: 22715-73-7
• Molecular Formula: C₁₄H₁₅N₃O₂
• Molecular Weight: 257.2878
• Mol File: 22715-73-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 391.2°C at 760 mmHg
• Flash Point: 190.4°C
• Density: 1.13g/cm³
• Vapor Pressure: 2.51E-06mmHg at 25°C
• Refractive Index: 1.563
• CAS DataBase Reference: (1E)-1,3-bis(4-methoxyphenyl)triaz-1-ene(CAS DataBase Reference)
• NIST Chemistry Reference: (1E)-1,3-bis(4-methoxyphenyl)triaz-1-ene(22715-73-7)
• EPA Substance Registry System: (1E)-1,3-bis(4-methoxyphenyl)triaz-1-ene(22715-73-7)

Safety Data

• Hazardous Substances Data: 22715-73-7(Hazardous Substances Data)

Usage

Description

(1E)-1,3-bis(4-methoxyphenyl)triaz-1-ene, also known as bis(4-methoxyphenyl)triazene, is a chemical compound that belongs to the class of triazenes. It is a yellow to orange crystalline solid that is insoluble in water but soluble in organic solvents.

Uses

Used in Colorant Industry:
(1E)-1,3-bis(4-methoxyphenyl)triaz-1-ene is used as a diazo component for the preparation of colorants, particularly azo dyes, due to its ability to undergo diazo coupling reactions.
Used in Antimicrobial Applications:
(1E)-1,3-bis(4-methoxyphenyl)triaz-1-ene is used as an antimicrobial agent due to its ability to exhibit antimicrobial and antifungal properties.
Used in Photodynamic Therapy:
(1E)-1,3-bis(4-methoxyphenyl)triaz-1-ene is used as a potential agent in photodynamic therapy for cancer treatment, as it has been investigated for its potential use in this field.
However, it should be handled with caution, as it is considered to be a potential occupational hazard and a possible environmental contaminant.

Upstream product

• 104-94-9 4-methoxy-aniline 
• 5416-93-3 4-Methoxyphenyl isocyanate 

Downstream Products

• 15637-10-2 Ag⁽¹⁺⁾*C₁₄H₁₄N₃O₂^(1-)={AgC₁₄H₁₄N₃O₂} 
• 54387-40-5 bis(1,3-di-p-methoxyphenyltriazenido)bis(triphenylphosphine)ruthenium(II) 
• 54387-41-6 carbonylhydrido(1,3-dimethoxyphenyltriazenido)bis(triphenylphosphine)ruthenium(II) 
• 295795-11-8 [Rh2(CO)4(μ-p-MeOC6H4NNNC6H4OMe-p)2] 
• 54387-41-6 C₅₁H₄₆N₃O₃P₂Ru 
• 696-63-9 4-Methoxybenzenethiol 
• 17333-79-8 p-methoxybenzenediazonium 
• 104-94-9 4-methoxy-aniline 
• 124914-59-6 1,3-bis(p-methoxyphenyl)triazenido-silver(I) 
• 10153-22-7 N-(4-methoxy-phenyl)-N'-p-tolyl-triazene 
• 110356-31-5 p-toluidino-ethenetricarbonitrile 
• 116083-06-8 tricyanovinylamine 

Relevant articles and documents

A New Reaction of Aryl Isocyanates with Nitrite Ion

Reaction of nitrite ion with excess aryl isocyanate in organic solvents at 0 deg C rapidly produces 1,3-diaryltriazenes in good yields via an aryldiazotate ion intermediate reacting with a second molecule of the aryl isocyanate.

Pd-catalyzed C-H activation/C-N bond formation: A new route to 1-aryl-1H-benzotriazoles

A method for the C-H activation of aryl triazene compounds followed by intramolecular amination is described. It involves the use of a catalytic amount of Pd(OAc)2 that efficiently effects the cyclization to provide 1-aryl-1H-benzotriazoles at moderate temperature.