4610-03-1 Usage
Description
2,5-Cyclohexadien-1-one, 4-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]imino]-2,6-bis(1,1-dimethylethyl)is a cyclohexadienone derivative characterized by its imino and hydroxy functional groups. It is a versatile chemical compound with potential applications in various industries due to its unique structure and properties.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 4610-03-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,1 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4610-03:
(6*4)+(5*6)+(4*1)+(3*0)+(2*0)+(1*3)=61
61 % 10 = 1
So 4610-03-1 is a valid CAS Registry Number.
4610-03-1Relevant 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
Fedulina,Klindukhov
, p. 692 - 698 (2007/10/03)
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.
INFLUENCE OF THE NATURE OF THE BASE ON THE OXIDATION OF 3,5-DI-tert-BUTYL-4-HYDROXYBENZALDEHYDE
Leineko, I. P.,Fedulina, T. G.,Pranovich, A. V.
, p. 113 - 117 (2007/10/02)
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 2,6-DI-tert-BUTYL-4-METHYLPHENOL BY OXYGEN IN AQUEOUS AMMONIA SOLUTION
Fedulina, T. G.,Deineko, I. P.,Zenkevich, I. G.,Zarubin, M. Ya.
, p. 1373 - 1377 (2007/10/02)
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).