761459-40-9

Usage

Uses

Used in Fragrance Industry:
1-Propanone, 1-(4-hydroxy-2-methylphenyl)-2-methylis used as a fragrance ingredient for its pleasant odor, contributing to the creation of various scent profiles in perfumes, colognes, and other fragrance products.
Used in Flavoring Industry:
In the flavoring industry, 1-Propanone, 1-(4-hydroxy-2-methylphenyl)-2-methylis utilized as a flavoring agent, enhancing the taste of food and beverages with its appealing flavor notes.
Used in Pharmaceutical Industry:
1-Propanone, 1-(4-hydroxy-2-methylphenyl)-2-methylserves as an essential component in the development and production of pharmaceuticals, given its properties that can contribute to the effectiveness and palatability of medications.
Used as a Precursor in Organic Synthesis:
In the field of organic synthesis, 1-Propanone, 1-(4-hydroxy-2-methylphenyl)-2-methylacts as a precursor for the synthesis of other complex organic compounds, further expanding its utility in the chemical industry.
Overall, 1-Propanone, 1-(4-hydroxy-2-methylphenyl)-2-methylis a versatile chemical compound with a wide range of applications across different industries, from enhancing sensory experiences in fragrances and flavorings to playing a crucial role in pharmaceutical development and organic synthesis. Its relative safety with proper handling and storage makes it a preferred choice for various applications.

Upstream product

• 108-39-4 3-methyl-phenol 
• 79-31-2 isobutyric Acid 
• 79-30-1 isobutyryl chloride 

Downstream Products

• 54696-07-0 4-methoxy-2-methylisobutyrophenone 

Relevant academic research and scientific papers

Preparation method of (4-isopropoxy-2-methyl)phenyl isopropyl ketone

The invention relates to a preparation method of (4-isopropoxy-2-methyl)phenyl isopropyl ketone. The preparation method specifically comprises the following steps: reacting m-cresol with thiocyanate under the action of a catalyst to obtain a product A; reacting the product A with halogenated isopropane under the action of an alkali and a catalyst to obtain a product B; carrying out a reaction on the product B and isopropyl magnesium halide, and carrying out a treatment to obtain the (4-isopropoxy-2-methyl)phenyl isopropyl ketone. The purity of prepared (4-isopropoxy-2-methyl)phenyl isopropyl ketone is 99% or above, and the total yield is 79% or above. According to the method, the use of toxic reagents and generation of a large amount of acid wastewater are avoided, the reaction temperatureis reduced, the reaction yield is increased, the process route is simple and efficient, the cost is reduced, the purity of the obtained product is high, the production safety is greatly improved, andindustrial popularization is facilitated.

FUNGICIDAL COMPOSITION CONTAINING ACID AMIDE DERIVATIVE

Conventional many fungicidal compositions have had practical problems such that either a preventive effect or a curing effect is inadequate, the residual effect tends to be inadequate, or the controlling effect against plant diseases tends to be inadequat

Improvement of Selectivity in the Fries Rearrangement and Direct Acylation Reactions by Means of P2O5/SiO2 Under Microwave Irradiation in Solvent-Free Media

P2O5/SiO2 was found to be an efficient new reagent for the Fries rearrangement of acyloxy benzene or naphthalene derivatives and the direct acylation reactions of phenol and naphthol derivatives with carboxylic acids. The reactions proceeded smoothly in the solid state and are highly selective methods for the preparation of the ortho isomers of hydroxyaryl ketones. Microwave irradiation improved the conversion yield to 85-100 percent and the high ortho-regioselectivity of these reactions provides an efficient and versatile procedure for obtaining o-hydroxyaryl ketones in 47-98 percent yield.