6698-70-0

Usage

Uses

Used in Fragrance and Flavor Industry:
1-(4-METHYLPHENOXY)-2-PROPANONE is used as a fragrance ingredient for its ability to enhance the scent of various products. It contributes to the creation of distinct and appealing aromas in the fragrance industry.
Used in Flavor Production:
In the flavor industry, 1-(4-METHYLPHENOXY)-2-PROPANONE is utilized to impart specific taste profiles to different products, making it a valuable component in the development of unique flavors.
Used as a Solvent in Industrial Applications:
1-(4-METHYLPHENOXY)-2-PROPANONE serves as a solvent in various industrial processes, where its solubility in organic solvents makes it a suitable candidate for dissolving substances and facilitating chemical reactions.
Used as a Solvent in Commercial Applications:
Similarly, in commercial applications, 1-(4-METHYLPHENOXY)-2-PROPANONE is employed as a solvent for its capacity to dissolve and interact with other compounds, making it a versatile component in the production of various products.

InChI:InChI=1/C10H12O2/c1-8-3-5-10(6-4-8)12-7-9(2)11/h3-6H,7H2,1-2H3

Upstream product

• 1121-70-6 sodium 4-methylphenoxide 
• 78-95-5 chloroacetone 
• 67-66-3 chloroform 
• 5471-86-3 (2'-methylallyl)(4-methyl-phenyl)aether 
• 10028-15-6 ozone 
• 106-44-5 p-cresol 
• 2684-62-0 diazoacetone 
• 75-56-9 methyloxirane 
• 23431-48-3 allyl p-tolyl ether 
• 4369-08-8 2-(4-methylphenoxy)-1-methylethan-1-ol 
• 5651-90-1 1-methyl-4-(2-propynyloxy)benzene 
• 598-31-2 1-bromoacetone 

Downstream Products

• 106-44-5 p-cresol 
• 18621-30-2 <4-Methyl-phenoxy>-aceton-dimethyl-ketal 
• 61711-87-3 1-methyl-2-p-methylphenoxyethylamine 
• 21571-68-6 <2-Chlormethyl-4-methyl-phenoxy>-aceton 

Relevant academic research and scientific papers

Selective Cross-Dehydrogenative C(sp3)-H Arylation with Arenes

Selective C(sp3)-C(sp2) bond construction is of central interest in chemical synthesis. Despite the success of classic cross-coupling reactions, the cross-dehydrogenative coupling between inert C(sp3)-H and C(sp2)-H bonds represents an attractive alternative toward new C(sp3)-C(sp2) bonds. Herein, we establish a selective inter-and intramolecular C(sp3)-H arylation of alcohols with nondirected arenes that thereby provides a general pathway to access a wide range of β-arylated alcohols, including tetrahydronaphthalen-2-ols and benzopyran-3-ols, with high to excellent chemo-and regioselectivity.

A (different) bright ammonia amide carbamate derivative and application thereof (by machine translation)

The invention belongs to the field of plant, relates to a general formula (I) is shown in a (different) bright ammonia amide carbamate derivatives and their pharmaceutically acceptable salt, wherein substituent R has the definition given in the specification, the invention also relates to the general formula (I) preparation of compounds of the, specifically for the preparation of the intermediate of its development and application of plant disease control. (by machine translation)

Wacker oxidation of terminal olefins in a mixture of [bmim][BF4] and water

A simple and efficient PdCl2/CuCl catalyzed oxidation of alkenes has been successfully developed using a mixture of water and the ionic liquid [bmim][BF4] as solvent. Starting from various types of terminal olefins, the corresponding ketones have been prepared under mild reaction conditions and obtained in good to excellent yields after a simple extraction with diethyl ether. Furthermore, it was possible to recycle and reuse the ionic liquid and the catalytic system.

Linear Free Energy Correlation Analysis on the Electronic Effects of Rh(II) Carbene O-H Insertion

The relative rate constants for the Rh(II)-catalyzed insertion of diazoacetone into the O-H bond have been measured through intermolecular competitions. The kinetic data were subjected to Hammett correlation analysis, and mechanistic implication of the results with respect to a stepwise vs a concerted O-H insertion pathway is discussed.

POLYMER-SUPPORTED REAGENTS: AN EFFICIENT METHOD FOR THE SYNTHESIS OF PHENOXYACETONES

Phenoxides supported on Amberlite IRA-400 reacted with chloroacetone to give the corresponding phenoxyacetones in high yields and purity.