4962-29-2

Basic information

• Product Name: Phenol, 4-methoxy-3,5-dimethyl-
• CAS NO: 4962-29-2
• Molecular Formula: C9H12O2
• Molecular Weight: 152.193
• Mol File: 4962-29-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Phenol, 4-methoxy-3,5-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 4-methoxy-3,5-dimethyl-(4962-29-2)
• EPA Substance Registry System: Phenol, 4-methoxy-3,5-dimethyl-(4962-29-2)

Safety Data

• Hazardous Substances Data: 4962-29-2(Hazardous Substances Data)

Usage

General Description

Phenol, 4-methoxy-3,5-dimethyl- is a synthetic compound that belongs to the family of phenols, which are organic compounds containing a hydroxyl group attached to an aromatic ring. With the chemical formula C9H12O2, this particular phenol has a molecular structure consisting of a phenol ring with a methoxy group at the 4th carbon position and methyl groups at the 3rd and 5th carbon positions. It is commonly used as a starting material in the synthesis of various pharmaceuticals, chemicals, and dyes due to its unique chemical properties and reactivity. Phenol, 4-methoxy-3,5-dimethyl- is also known for its antimicrobial and antioxidant properties, making it a valuable ingredient in skincare and personal care products.

Upstream product

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

Downstream Products

• 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 
• 39785-37-0 4-amino-2,6-dimethylanisole 
• 158815-51-1 2-methoxy-1,3-dimethyl-5-nitrosobenzene 
• 37570-33-5 4-methoxy-3,5-dimethylphenyl acetate 
• 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 
• 2055-82-5 4-(4-Methoxy-3,5-dimethyl-phenoxy)-3,5-dinitro-phenylessigsaeure-methylester 

Relevant articles and documents

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.

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.

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