35050-88-5

Usage

Uses

Used in Medicinal and Personal Care Products:
Thymol is used as an antiseptic and antifungal agent in medicinal and personal care products, such as mouthwashes, hand sanitizers, and topical antifungal creams. Its ability to destroy and inhibit the growth of microorganisms makes it an effective ingredient in these products.
Used in Food and Beverages:
Thymol is used as a flavoring agent in food and beverages, adding a unique taste and aroma to various products.
Used in Agriculture:
In the agricultural industry, thymol is used as a natural pesticide due to its ability to control and prevent the growth of harmful microorganisms and pests.
Used in Perfumes and Cosmetics Manufacturing:
Thymol is utilized in the manufacturing of perfumes and cosmetics for its pleasant aroma and as a preservative to maintain the freshness and longevity of the products.

InChI:InChI=1/C11H16O/c1-4-9-6-8(3)7-10(5-2)11(9)12/h6-7,12H,4-5H2,1-3H3

Upstream product

• 106-44-5 p-cresol 
• 74-85-1 ethene 
• 81591-15-3 3'-ethyl-5'-methyl-2'-hydroxy-acetophenone 
• 64-17-5 ethanol 
• 24544-08-9 2,6-diethyl-4-methylaniline 
• 19125-76-9 3-dimethylamino-2-methyl-acrylaldehyde 
• 5331-82-8 2-ethyl-3-oxohexanoic acid ethyl ester 
• 123-19-3 4-heptanone 
• 42588-57-8 3-ethoxymethacrolein 
• 78-85-3 2-methylpropenal 
• 1612866-71-3 1,3-diethyl-2-methoxy-5-methylbenzene 
• 1612866-70-2 1,3-diethynyl-2-methoxy-5-methylbenzene 
• 51699-89-9 1,3-dibromo-2-methoxy-5-methylbenzene 
• 2432-14-6 3,5-dibromo-4-hydroxytoluene 

Downstream Products

• 854435-87-3 2,6-diethyl-4-methyl-cyclohexanol 

Relevant academic research and scientific papers

Novel process for synthesizing high-steric-hindrance bromobenzene

The invention relates to a novel process for synthesizing high-steric-hindrance bromobenzene. A preparing method of aryl bromide includes the steps of conducting reaction on aniline hydrobromide and inorganic nitrite in a two-phase or multi-phase system f

Preparation method of multi-substituted phenol

The invention provides a preparation method of multi-substituted phenol. According to the preparation method, raw materials, namely alkyl ketone and alkene, are subjected to condensation-aromatizationunder action of a catalyst to obtain multi-substituted phenol. Compared with the prior art, the preparation method has the advantages that the raw materials are easy to obtain, the yield is high, cost is low since use of expensive metallic catalysts is avoided, and the preparation method is suitable for industrial production and the like.

Three-component asymmetric catalytic ugi reaction - Concinnity from diversity by substrate-mediated catalyst assembly

The first chiral catalyst for the three-component Ugi reaction was identified as a result of a screen of a large set of different BOROX catalysts. The BOROX catalysts were assembled in situ from a chiral biaryl ligand, an amine, water, BH3×SMe2, and an alcohol or phenol. The catalyst screen included 13 different ligands, 12 amines, and 47 alcohols or phenols. The optimal catalyst system (LAP 8-5-47) provided α-amino amides from an aldehyde, a secondary amine, and an isonitrile with excellent asymmetric induction. The catalytically active species is proposed to be an ion pair that consists of the chiral boroxinate anion and an iminium cation. Harmonious arrangement of parts: A screen of BOROX catalysts that were generated in situ from 13 different ligands and 47 alcohols led to the identification of an effective combination for the catalytic asymmetric three-component Ugi reaction. Experimental results suggest that the catalyst is a chiral polyborate anion, which then forms an ion pair with the iminium cation that is generated from aldehyde and secondary amine.

Halide-free ethylation of phenol by multifunctional catalysis using phosphinite ligands

The ortho-alkylation of phenols or aniline by catalytic C-H activation and multifunctional catalysis is described. The Royal Society of Chemistry 2006.

Catalytic ethylation of phenols

Alkylation of phenol and cresols with ethanol in the presence of iron-aluminum catalyst was studied.