2178-51-0

Basic information

• Product Name: 2,5-Cyclohexadien-1-one, 4-[3,5-bis(1-methylethyl)-4-oxo-2,5-cyclohexadien-1-ylidene]-2,6-bis(1- methylethyl)-
• CAS NO: 2178-51-0
• Molecular Formula: C24H32O2
• Molecular Weight: 352.517
• Mol File: 2178-51-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2,5-Cyclohexadien-1-one, 4-[3,5-bis(1-methylethyl)-4-oxo-2,5-cyclohexadien-1-ylidene]-2,6-bis(1- methylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Cyclohexadien-1-one, 4-[3,5-bis(1-methylethyl)-4-oxo-2,5-cyclohexadien-1-ylidene]-2,6-bis(1- methylethyl)-(2178-51-0)
• EPA Substance Registry System: 2,5-Cyclohexadien-1-one, 4-[3,5-bis(1-methylethyl)-4-oxo-2,5-cyclohexadien-1-ylidene]-2,6-bis(1- methylethyl)-(2178-51-0)

Safety Data

• Hazardous Substances Data: 2178-51-0(Hazardous Substances Data)

Usage

General Description

2,5-Cyclohexadien-1-one, 4-[3,5-bis(1-methylethyl)-4-oxo-2,5-cyclohexadien-1-ylidene]-2,6-bis(1-methylethyl)-, is a chemical compound with a complex molecular structure. It contains a cyclohexadienone ring with multiple methyl groups attached. The presence of the carbonyl group and the cyclohexadienylidene moiety suggests that this compound may have potential biological or chemical reactivity. It is important to handle this compound with caution, as its precise properties and potential uses or hazards are not readily apparent without further analysis.

Upstream product

• 2416-95-7 3,3',5,5'-tetraisopropyl-[1,1'-biphenyl]-4,4'-diol 
• 2078-54-8 2,6-diisopropylphenol 

Downstream Products

• 2416-95-7 3,3',5,5'-tetraisopropyl-[1,1'-biphenyl]-4,4'-diol 
• 1988-11-0 2,6-diisopropyl-1,4-benzoquinone 

Relevant articles and documents

Solubilization of dipropofol, an antibacterial agent, using saccharide and ascorbic acid

Dipropofol has a strong antibacterial activity against Gram-positive bacteria. However, it lacked the solubility in water and this property was supposed to limit its efficacy. We tried to improve the solubility and found a new solubilization method of dipropofol in water by the addition of a monosaccharide or ascorbic acid.

Oxidative coupling of some 2,6-disubstituted phenol derivatives in perchloric acid mediated by cerium(IV) ions

2,6-Disubstituted phenol derivatives have been oxidized by cerium(IV) perchlorate in aqueous or aqueous-acetonitrile solutions of perchloric acid as well as in two-phase systems to the corresponding 1,4-benzoquinones, 4,4′-diphenoquinones, and oligomeric

Mushroom tyrosinase catalysed coupling of hindered phenols: A novel approach for the synthesis of diphenoquinones and bisphenols

An efficient oxidative carbon-carbon coupling of hindered phenols leading to diphenoquinones and bisphenols by mushroom tyrosinase is reported.