4610-03-1

Basic information

• Product Name: 2,5-Cyclohexadien-1-one, 4-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]imino]-2,6-bis(1,1-dimeth ylethyl)-
• CAS NO: 4610-03-1
• Molecular Formula: C28H41NO2
• Molecular Weight: 423.639
• Mol File: 4610-03-1.mol

Chemical Properties

• CAS DataBase Reference: 2,5-Cyclohexadien-1-one, 4-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]imino]-2,6-bis(1,1-dimeth ylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Cyclohexadien-1-one, 4-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]imino]-2,6-bis(1,1-dimeth ylethyl)-(4610-03-1)
• EPA Substance Registry System: 2,5-Cyclohexadien-1-one, 4-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]imino]-2,6-bis(1,1-dimeth ylethyl)-(4610-03-1)

Safety Data

• Hazardous Substances Data: 4610-03-1(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
2,5-Cyclohexadien-1-one, 4-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]imino]-2,6-bis(1,1-dimethylethyl)is used as an intermediate in the synthesis of various pharmaceuticals. Its unique structure and functional groups make it a valuable building block for the development of new drugs with diverse therapeutic properties.
Used in Polymer Industry:
2,5-Cyclohexadien-1-one,
4-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]imino]-2,6-bis(1,1-dimeth
ylethyl)is also used in the production of polymers, where its bis(1,1-dimethylethyl) groups provide solubility and stability. Its incorporation into polymer structures can enhance their mechanical, thermal, and chemical properties, making them suitable for various applications, such as coatings, adhesives, and plastics.
Used in Cosmetics and Personal Care Products:
Due to its potential antioxidant properties, 2,5-Cyclohexadien-1-one, 4-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]imino]-2,6-bis(1,1-dimethylethyl)can be used in the formulation of cosmetics and personal care products. Its antioxidant activity may help protect the skin from oxidative stress and environmental damage, promoting skin health and appearance.
Used in Industrial Applications:
2,5-Cyclohexadien-1-one,
4-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]imino]-2,6-bis(1,1-dimeth
ylethyl)-'s versatility and stability make it suitable for various industrial applications, such as lubricants, fuel additives, and other specialty chemicals. Its unique structure and properties can contribute to improved performance and efficiency in these applications.

Upstream product

• 2700-36-9 Tetra-tert-butylindophenoxyl 
• 1707-75-1 2,2-diphenyl-1-picrylhydrazine 
• 128-37-0 2,6-di-tert-butyl-4-methyl-phenol 
• 1620-98-0 3,5-di-t-butyl-4-hydroxybenzaldehyde 
• 88-26-6 3,5-di-tert-butyl-4-hydroxybenzyl alcohol 
• 87-97-8 2,6-di-tert-butyl-4-methoxymethylene-phenol 
• 719-22-2 2,6-Di-tert-butyl-1,4-benzoquinone 
• 950-58-3 2,6-di-tert-butyl-4-aminophenol 
• 728-40-5 4-nitro-2,6-di-tert-butylphenol 
• 4359-97-1 2,6-di-tert-butyl-4-(3,5-di-tert-butyl-4-hydroxy-benzylidene)-cyclohexa-2,5-dienone 

Downstream Products

• 15463-88-4 2,6-Di-tert.butyl-4-(3,5-di-tert.butyl-4-oxo-cyclohedien-(2,5)-ylidenamino)-phenolat 
• 950-58-3 2,6-di-tert-butyl-4-aminophenol 
• 132668-95-2 2,6-Di-tert-butyl-4-(3,5-di-tert-butyl-4-methoxy-phenylimino)-cyclohexa-2,5-dienone 
• 124980-85-4 C₂₉H₄₃NO₂ 
• 69230-90-6 3,5-di-tert-butyl-4-hydroxyformanilide 
• 2700-36-9 Tetra-tert-butylindophenoxyl 
• 4359-97-1 2,6-di-tert-butyl-4-(3,5-di-tert-butyl-4-hydroxy-benzylidene)-cyclohexa-2,5-dienone 
• 1707-75-1 2,2-diphenyl-1-picrylhydrazine 

Relevant articles and documents

Reactivity of 3,5-di-tert-butyl-4-hydroxybenzaldehyde, 3,5-di-tert-butyl-4-hydroxybenzyl alcohol, and (3,5-di-tert-butyl-4-hydroxybenzyl)methyl ether at oxidation by oxygen in basic solutions

Reactivity at oxidation in basic water-ethanol solutions of the fallowing phenols: 3,5-di-tert-butyl-4-hydroxybenzaldehyde, 3,5-di-tert-butyl-4-hydroxybenzyl alcohol, and (3,5-di-tert-butyl-4-hydroxybenzyl)methyl ether was studied as affected by α-located oxygen-containing functional groups and the base nature. It is shown that the substrate reactivity drops in the order: alcohol ≥ ether > aldehyde. In the presence of NaOH, Na2CO3, and NaHCO3 the alcohol and the ether are similar in efficiency, while in aqueous ammonia the alcohol reactivity is much higher than that of ether. Aldehyde oxidizes in ammoniak with the tenfold faster than in solutions of NaOH, Na2CO3, and NaHCO3.

Reactions of isomeric 3,6- and 3,5-di-tert-butyl-ortho-benzoquinones

The interaction of 3,6-di-tert-butyl-ortho-benzoquinone (1) and 3,5-di-tert-butyl-ortho-benzoquinone (2) with NH3 in water-alcohol medium and with (NH4)2 CO3 in a solid phase has been studied.Redox processes with participation of a nucleophile of the medi

INFLUENCE OF THE NATURE OF THE BASE ON THE OXIDATION OF 3,5-DI-tert-BUTYL-4-HYDROXYBENZALDEHYDE

One course of reaction in the oxidation of 3,5-di-tert-butyl-4-hydroxybenzaldehyde is the elimination of formyl in the form of formic acid and the formation of 2,6-di-tert-butyl-p-benzoquinone; in a medium of NH4OH the oxidation is accelerated on account of the formation of 3,5-di-tert-butyl-4-hydroxybenzaldehyde imine, which is oxidized more readily than the original carbonyl compound.

OXIDATION OF 3,5-DI-tert-BUTYL-4-HYDROXYBENZYL ALCOHOL AND 3,5-DI-tert-BUTYL-4-HYDROXYBENZALALDEHYDE BY OXYGEN IN AQUEOUS AMMONIUM SOLUTION

The main reaction products during the oxidation of 3,5-di-tert-butyl-4-hydroxy-benzyl alcohol and 3,5-di-tert-butyl-4-hydroxybenzaldehyde by oxygen in a waterpropanol solution of ammonia are 3,3',5,5'-tetra-tert-butyldiphenoquinone, 2,6-di-tert-butyl-1,4-benzoquinone, and 3,3'5,5'-tetra-tert-butylindophenol, which is formed in the reaction of the above-mentioned p-benzoquinone with ammonia.Three nitrogen containing substances were also found in the products from the oxidative ammonolysis of the aldehyde, i.e., 2,6-di-tert-butyl-4-cyanophenol, 2,6-di-tert-butyl-4--2,5-cyclohexadien-1-one, and a third compound with a molecular mass of 490, for which the elemental composition was determined.

OXIDATION OF 2,6-DI-tert-BUTYL-4-METHYLPHENOL BY OXYGEN IN AQUEOUS AMMONIA SOLUTION

Both monomeric and dimeric oxidation products are formed during the oxidation of 2,6-di-tert-butyl-4-methylphenol (ionole) by oxygen in a water-propanol solution of ammonia.Two nitrogen-containing compounds 3,3'-5,5'-tetra-tert-butylindophenol and 2,6-di-tert-butyl-4-cyanophenol are also formed, and their amounts in the reaction mixture increase with increase in temperature (45-120 deg C).