3796-87-0

Usage

General Description

2,3-dimethyl-6-(prop-2-en-1-yl)phenol, also known as eugenol, is a naturally occurring chemical compound found in various plants such as cloves, basil, cinnamon, and bay leaves. It is commonly used in perfumes, flavorings, and essential oils due to its pleasant, spicy aroma. Eugenol also possesses antibacterial, antifungal, and analgesic properties, making it a popular ingredient in dental products, insect repellents, and medicinal ointments. Additionally, it has been studied for its potential anti-inflammatory and antioxidant effects, suggesting possible therapeutic applications in the treatment of various diseases and conditions. However, eugenol can be toxic in high doses and should be used with caution.

Upstream product

• 526-75-0 2,3-Dimethylphenol 
• 3731-94-0 allyl 2,3-dimethylphenyl ether 
• 20700-85-0 5,6-dimethyl-6-allcyclohexa-2,4-diene-1-one 

Downstream Products

• 182010-87-3 2,3-dimethyl-4-nitro-6-(2-propenyl)phenol 
• 182010-88-4 (E)-6-(2-methoxy-3,4-dimethyl-5-nitrophenyl)-4-methyl-4-hexenoic acid 
• 182010-85-1 1-Allyl-5-bromo-2-methoxy-3,4-dimethyl-benzene 
• 182010-84-0 4-bromo-2,3-dimethyl-6-(2-propenyl)phenol 
• 869468-97-3 trifluoro-methanesulfonic acid 6-(2-methoxycarbonyloxy-ethyl)-2,3-dimethyl-phenyl ester 

Relevant academic research and scientific papers

A domino amidation route to indolines and indoles: Rapid syntheses of anhydrolycorinone, hippadine, oxoassoanine, and pratosine

(Chemical Equation Presented) When subjected to palladium-catalyzed amidation conditions, 2-triflyloxy phenethyl carbonates undergo, in addition to the expected aryl cross-coupling, an additional amidation with net displacement of the carbonate. The result is a one-step synthesis of indolines which may be oxidized to indoles. The utility of the procedure is illustrated by the two- or three-step syntheses of anhydrolycorinone, hippadine, oxoassoanine, and pratosine.

Structure-activity relationships for inhibition of inosine monophosphate dehydrogenase by nuclear variants of mycophenolic acid

Structure-activity relationships in the region of the phthalide ring of the inosine monophosphate dehydrogenase inhibitor mycophenolic acid have been explored. Replacement of the lactone ring with other cyclic moieties resulted in loss of potency, especia

929. Chrom-3-en-6-ols. The action of pyridine on alk-2-enyl-benzoquinones

Allylbenzoquinones are converted by treatment with pyridine into quinols and chrom-3-en-6-ols. The tendency for the latter reaction to occur increases as the benzoquinone ring becomes more highly substituted.