30876-55-2

Basic information

• Product Name: 2,5-Cyclohexadiene-1,4-dione, 2-(3-hydroxy-3-methylbutyl)-3,5,6-trimethyl-
• CAS NO: 30876-55-2
• Molecular Formula: C14H20O3
• Molecular Weight: 236.311
• Mol File: 30876-55-2.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2,5-Cyclohexadiene-1,4-dione, 2-(3-hydroxy-3-methylbutyl)-3,5,6-trimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Cyclohexadiene-1,4-dione, 2-(3-hydroxy-3-methylbutyl)-3,5,6-trimethyl-(30876-55-2)
• EPA Substance Registry System: 2,5-Cyclohexadiene-1,4-dione, 2-(3-hydroxy-3-methylbutyl)-3,5,6-trimethyl-(30876-55-2)

Safety Data

• Hazardous Substances Data: 30876-55-2(Hazardous Substances Data)

Upstream product

• 950-99-2 2,2,5,7,8-pentamethylchroman-6-ol 
• 64-17-5 ethanol 
• 7705-08-0 iron(III) chloride 
• 71-43-2 benzene 
• 94-36-0 dibenzoyl peroxide 
• 92014-26-1 8a-hydroperoxy-2,2,5,7,8-pentamethylchroman-6(8aH)-one 
• 24165-02-4 8a-hydroxy-2,2,5,7,8-pentamethylchroman-6(8aH)-one 
• 119529-12-3 8a-methoxy-2,2,5,7,8-pentamethylchroman-6-one 
• 67-56-1 methanol 
• 563-63-3 silver(I) acetate 

Downstream Products

• 950-99-2 2,2,5,7,8-pentamethylchroman-6-ol 

Relevant articles and documents

RUTHENIUM-CATALYZED OXIDATION OF PHENOLS WITH HYDROGEN PEROXIDE

RuCl3 catalyzed the oxidation of trimethylphenol with 30percent H2O2 in acidic medium to give the corresponding p-bezoquinone in high yield.

Investigation into phenoxonium cations produced during the electrochemical oxidation of chroman-6-ol and dihydrobenzofuran-5-ol substituted compounds

(Chemical Equation Presented) A series of chroman-6-ol and dihydrobenzofuran-5-ol based compounds with structures similar to vitamin E were examined by cyclic voltammetry and controlled potential electrolysis. The compounds displayed characteristic voltammetric features that enabled their electrochemical behavior to be interpreted in relation to the oxidation mechanism for vitamin E. The electrochemical experiments indicated the presence of several oxidized species: cation radicals, phenoxyl radicals, phenoxonium ions, hemiketals, and p-quinones, whose lifetimes varied depending on the extent of methylation of the aromatic ring (R1, R2, R3) and the nature of substituents R4 and R5.

Reaction of 2,2,5,7,8-pentamethyl-6-chromanol, an α-tocopherol analogue, with NO in the presence of oxygen

An α-tocopherol model compound, 2,2,5,7,8-pentamethyl-6-chromanol, reacted with nitric oxide (NO) in the presence of various amounts of oxygen to afford four major products. Distribution of the products was varied depending on the ratio of NO and O2