41684-39-3

Basic information

• Product Name: (4E)-2,5-bis[(4-methylphenyl)amino]-4-[(4-methylphenyl)imino]cyclohexa-2,5-dien-1-one
• Synonyms: (4E)-2,5-Bis[(4-methylphenyl)amino]-4-[(4-methylphenyl)imino]cyclohexa-2,5-dien-1-one; 2,5-cyclohexadien-1-one, 2,5-bis[(4-methylphenyl)amino]-4-[(4-methylphenyl)imino]-, (4E)-
• CAS NO: 41684-39-3
• Molecular Formula: C₂₇H₂₅N₃O
• Molecular Weight: 407.5069
• Mol File: 41684-39-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 566.9°C at 760 mmHg
• Flash Point: 296.7°C
• Density: 1.12g/cm³
• Vapor Pressure: 7.18E-13mmHg at 25°C
• Refractive Index: 1.615
• CAS DataBase Reference: (4E)-2,5-bis[(4-methylphenyl)amino]-4-[(4-methylphenyl)imino]cyclohexa-2,5-dien-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: (4E)-2,5-bis[(4-methylphenyl)amino]-4-[(4-methylphenyl)imino]cyclohexa-2,5-dien-1-one(41684-39-3)
• EPA Substance Registry System: (4E)-2,5-bis[(4-methylphenyl)amino]-4-[(4-methylphenyl)imino]cyclohexa-2,5-dien-1-one(41684-39-3)

Safety Data

• Hazardous Substances Data: 41684-39-3(Hazardous Substances Data)

Usage

Description

(4E)-2,5-bis[(4-methylphenyl)amino]-4-[(4-methylphenyl)imino]cyclohexa-2,5-dien-1-one is a complex organic compound characterized by its cyclohexa-2,5-dien-1-one core structure. It features two amino groups and one imino group, all attached to the cyclohexadienone ring, along with two 4-methylphenyl groups connected to the amino and imino groups. This unique structure and the presence of various functional groups indicate its potential for applications in organic synthesis and pharmaceutical research.

Uses

Used in Organic Synthesis:
(4E)-2,5-bis[(4-methylphenyl)amino]-4-[(4-methylphenyl)imino]cyclohexa-2,5-dien-1-one is used as a key intermediate for the synthesis of various organic compounds due to its reactive functional groups and unique molecular structure.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (4E)-2,5-bis[(4-methylphenyl)amino]-4-[(4-methylphenyl)imino]cyclohexa-2,5-dien-1-one is used as a starting material for the development of novel drugs, leveraging its versatile chemical structure and functional groups to create potential therapeutic agents.
Further studies and analysis are required to fully comprehend the compound's properties and explore its potential uses in various applications.

Upstream product

• 106-49-0 p-toluidine 
• 120-80-9 benzene-1,2-diol 
• 106-51-4 p-benzoquinone 
• 18440-54-5 N-(4-Methylphenyl)-1,4-benzoquinone monoimine 

Relevant articles and documents

Metal ion promoted tautomerization and C-N bond cleavage: Conversion of catechol to a p-benzoquinone derivative

Metal ion promoted tautomerization of p-iminoquinone to o-diiminoquinone and a C-N bond cleavage of 2,5-bis(p-tolylamino)-4-p-tolyliminobenzoquinone leading to the conversion of catechol to a p-benzoquinone derivative are reported. This journal is

Unusual Reaction of N-(p-Tolyl)-1,4-benzoquinonemonoimine with p-Toluidine

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