4962-29-2

Usage

Uses

Used in Pharmaceutical Industry:
Phenol, 4-methoxy-3,5-dimethylis utilized as a starting material in the synthesis of various pharmaceuticals due to its unique chemical properties and reactivity. It plays a crucial role in the development of new drugs and medicines.
Used in Chemical Industry:
This phenolic compound is also employed as a starting material in the synthesis of various chemicals, including dyes, due to its reactivity and chemical properties. It contributes to the production of a wide range of chemical products.
Used in Skincare and Personal Care Products:
Phenol, 4-methoxy-3,5-dimethylis used as an ingredient in skincare and personal care products, capitalizing on its antimicrobial and antioxidant properties. It helps to protect the skin from harmful effects of free radicals and supports the development of products with enhanced efficacy and safety.
Used in Antimicrobial Applications:
Due to its antimicrobial properties, Phenol, 4-methoxy-3,5-dimethylis employed in various applications to inhibit the growth of microorganisms, contributing to the preservation and safety of different products.
Used in Antioxidant Formulations:
Leveraging its antioxidant properties, Phenol, 4-methoxy-3,5-dimethylis incorporated into formulations to protect against oxidative stress and support overall health and well-being.

Upstream product

• 77-78-1 dimethyl sulfate 
• 108-68-9 3,5-Dimethylphenol 
• 880-06-8 4-hydroxy-3,5-dimethylphenyl acetate 
• 10181-98-3 5-(2,6-dimethyl-phenoxy)-2-methoxy-1,3-dimethyl-benzene 
• 654-42-2 1,4-dihydroxy-2,6-dimethylbenzene 
• 14804-38-7 5-bromo-2-methoxy-1,3-dimethylbenzene 
• 7218-21-5 6-acetoxy-2,6-dimethyl-2,4-cyclohexadienone 
• 2233-18-3 4-hydroxy-3,5-dimethylbenzaldehyde 
• 67-56-1 methanol 
• 1004-66-6 2-methoxy-1,3-dimethylbenzene 

Downstream Products

• 14538-50-2 1,3-dimethyl-2,5-dimethoxybenzene 
• 2055-82-5 4-(4-Methoxy-3,5-dimethyl-phenoxy)-3,5-dinitro-phenylessigsaeure-methylester 
• 742-63-2 3,5-Diiod-4-(4-methoxy-3,5-dimethyl-phenoxy)-phenylessigsaeure 
• 1047-85-4 3,5-Diiod-4-(4-methoxy-3,5-dimethyl-phenoxy)-phenylessigsaeure-methylester 
• 37570-33-5 4-methoxy-3,5-dimethylphenyl acetate 
• 158815-51-1 2-methoxy-1,3-dimethyl-5-nitrosobenzene 
• 39785-37-0 4-amino-2,6-dimethylanisole 
• 116760-59-9 4,4-dimethoxy-3,5-dimethylcyclohexa-2,5-dien-1-one 
• 1431793-62-2 C₁₈H₂₂O₅ 
• 1026582-99-9 3,5-dichloro-2,3',6,6'-tetramethoxy-2',4'-dimethylbenzophenone 
• 146984-67-0 3,5-dichloro-2,3',6'-trihydroxy-6-methoxy-2',4'-dimethylbenzophenone 

Relevant academic research and scientific papers

Synthetic method 4 - alkoxyphenol compounds

The invention discloses a synthetic method of 4 - alkoxyphenol compounds, and belongs to the field of organic chemical synthesis. The method is as follows: An aryl alkyl ether compound is added to the sealing tube. The catalyst dimerization acetic acid rhodium and the oxidizing agent iodobenzene diethyl ester are added, a solvent trifluoroacetic anhydride is added, and the 4 -alkoxyphenol compound is prepared by heating reaction. To the invention, high regioselectivity direct hydroxylation of the aryl alkyl ether compound is realized, the application range of the substrate is wide, the yield is high, the activity after amplification reaction does not significantly decay, and higher yield is still obtained. The utility model has good practicability and industrial application prospect.

Para -Selective hydroxylation of alkyl aryl ethers

para-Selective hydroxylation of alkyl aryl ethers is established, which proceeds with a ruthenium(ii) catalyst, hypervalent iodine(iii) and trifluoroacetic anhydride via a radical mechanism. This protocol tolerates a wide scope of substrates and provides a facile and efficient method for preparing clinical drugs monobenzone and pramocaine on a gram scale.

Direct synthesis of anilines and nitrosobenzenes from phenols

A one-pot synthesis of anilines and nitrosobenzenes from phenols has been developed using an ipso-oxidative aromatic substitution (iSOAr) process. The products are obtained in good yields under mild and metal-free conditions. The leaving group effect on reactions that proceed through mixed quionone monoketals has also been investigated and a predictive model has been established.

Photocatalytic synthesis of dihydrobenzofurans by oxidative [3+2] cycloaddition of phenols

We report a protocol for oxidative [3+2] cycloadditions of phenols and alkenes applicable to the modular synthesis of a large family of dihydrobenzofuran natural products. Visible-light-activated transition metal photocatalysis enables the use of ammonium persulfate as an easily handled benign terminal oxidant. The broad range of organic substrates that are readily oxidized by photoredox catalysis suggests that this strategy may be applicable to a variety of useful oxidative transformations.

Gold-catalyzed dearomative spirocyclization of aryl alkynoate esters

Aryl alkynoate esters undergo gold-catalyzed spirocyclization under mild conditions, affording spirolactones in high yields. This approach obviates the need for stoichiometric halogenating reagents typically employed for alkyne activation in related trans

Selective one-pot synthesis of various phenols from diarylethanes

Various substituted phenols were selectively synthesized by a one-pot reaction through the NHPI-catalyzed aerobic oxidation of 1,1-diarylethanes followed by treatment with dilute sulfuric acid. The Royal Society of Chemistry.