1654-14-4

Basic information

• Product Name: 2,5-Cyclohexadiene-1,4-dione, 2,5-bis(methylamino)-
• CAS NO: 1654-14-4
• Molecular Formula: C8H10N2O2
• Molecular Weight: 166.18
• Mol File: 1654-14-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,5-Cyclohexadiene-1,4-dione, 2,5-bis(methylamino)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Cyclohexadiene-1,4-dione, 2,5-bis(methylamino)-(1654-14-4)
• EPA Substance Registry System: 2,5-Cyclohexadiene-1,4-dione, 2,5-bis(methylamino)-(1654-14-4)

Safety Data

• Hazardous Substances Data: 1654-14-4(Hazardous Substances Data)

Usage

Use

Building block in organic synthesis

Potential applications

Production of pharmaceuticals and organic materials, antioxidant properties, dye sensitizer in solar cells

Additional research

Development of new compounds for medical and industrial purposes

Upstream product

• 123-31-9 hydroquinone 
• 74-89-5 methylamine 
• 3117-03-1 2,5-dimethoxyquinone 
• 64-17-5 ethanol 
• 106-51-4 p-benzoquinone 
• 614-13-1 2-methoxy-5-methyl-1,4-benzoquinone 
• 21772-24-7 1,16-Bis-(2,5-dihydroxyphenyl)-hexadecan 
• 21772-23-6 1,16-Bis-(2,5-dimethoxyphenyl)-hexadecan 
• 21772-21-4 1.14-Bis-<2.5-dimethoxy-benzoyl>-tetradecan 
• 150-78-7 1,4-dimethoxybezene 
• 2425-81-2 phen-1,4-ylenbis(magnesiumbromid) 
• 2880-58-2 2-methoxy-1,4-benzoquinone 
• 21772-25-8 1,16-Bis-<1,4-benzochinonyl-(2)>-hexadecan 
• 4612-26-4 1,4-Phenyldiboronic acid 

Downstream Products

• 615-94-1 2,5-dihydroxy-1,4-benzoquinone 

Relevant articles and documents

Antiureolytic Activity of Substituted 2,5-Diaminobenzoquinones

A series of 2,5-bis(alkyl/arylamino)-1,4-benzoquinones (1–12) were investigated in vitro for their potential to inhibit the activity of jack bean urease. Compounds 1–6, 8, 9, 11 and 12 effectively inhibited the jack bean urease activity by 90.8 % when tes

2-(N-Alkyl-p-hydroxyanilino)-1,4-benzoquinones from p-Benzoquinones and Primary Aliphatic Amines. Studies on Quinones VI

In acetic (aqueous or chloroform) solution p-benzoquinones yield with primary aliphatic amines mainly 2-(N-alkyl-p-hydroxy-anilino)-1,4-benzoquinones besides the 2-alkylamino- and 2,5-bis(alkylamino)-quinones.The methyl-, ethyl-, n-propyl-, n-butylhomologues of p-benzoquinone and the isomer methylderivatives of toluquinone are described.Their structure were established by spectroscopic (UV/VIS, IR, NMR) methods and by synthesis of the methylderivative 3a from p-benzoquinone and p-hydroxy-N-methyl-aniline.The influence of other acids on the reaction was studied. - Keywords: N-Alkyl-p-hydroxyanilino-1,4-quinones; Quinones; Solvent influence