144150-79-8

Usage

Uses

Used in Pharmaceutical Manufacturing:
Phenol, 2-methoxy-4-(2-propenyl)-, 4-methylbenzenesulfonate is used as a catalyst or intermediate for the synthesis of various pharmaceutical compounds. Its role in these processes is crucial for the production of a range of medications, contributing to the development of new and existing treatments.
Used in Agrochemical Manufacturing:
Similarly, in the agrochemical industry, Phenol, 2-methoxy-4-(2-propenyl)-, 4-methylbenzenesulfonate serves as a catalyst or intermediate, facilitating the synthesis of various agrochemicals. Its application in this field is essential for the production of substances that protect crops and enhance agricultural productivity.
Used as a Reagent for Chemical Synthesis:
Phenol, 2-methoxy-4-(2-propenyl)-, 4-methylbenzenesulfonate is also utilized as a reagent in chemical synthesis, where it aids in the formation of desired products through various chemical reactions. Its versatility in this capacity makes it a valuable component in the synthesis of a wide array of chemical products.
Safety and Handling:
It is imperative to handle Phenol, 2-methoxy-4-(2-propenyl)-, 4-methylbenzenesulfonate with care due to its potential toxicity and the risk of causing irritation to the skin, eyes, and respiratory system. Proper management and storage in a well-ventilated area, along with the use of appropriate personal protective equipment, are essential to ensure the safety of those working with Phenol, 2-methoxy-4-(2-propenyl)-, 4-methylbenzenesulfonate.

Upstream product

• 97-53-0 4-allylguaiacol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 1335401-17-6 4-allyl-2-(methoxy-d₃)-phenol 
• 1229610-97-2 (E)-2-methoxy-4-(prop-1-en-1-yl)phenyl 4-methylbenzenesulfonate 
• 97-53-0 4-allylguaiacol 
• 62103-69-9 3-propylanisole 

Relevant academic research and scientific papers

Synergistic interactions of eugenol-Tosylate and its congeners with fluconazole against candida albicans

We previously reported the antifungal properties of a monoterpene phenol "Eugenol" against different Candida strains and have observed that the addition of methyl group to eugenol drastically increased its antimicrobial potency. Based on the results and t

A Next-Generation Air-Stable Palladium(I) Dimer Enables Olefin Migration and Selective C?C Coupling in Air

We report a new air-stable PdI dimer, [Pd(μ-I)(PCy2tBu)]2, which triggers E-selective olefin migration to enamides and styrene derivatives in the presence of multiple functional groups and with complete tolerance of air. The same dimer also triggers extremely rapid C?C coupling (alkylation and arylation) at room temperature in a modular and triply selective fashion of aromatic C?Br, C?OTf/OFs, and C?Cl bonds in poly(pseudo)halogenated arenes, displaying superior activity over previous PdI dimer generations for substrates that bear substituents ortho to C?OTf.

PROCESS FOR THE PREPARATION AND IDENTIFICATION OF DEUTERATED EUGENOL

The present invention provides a novel, simple, unique and viable processes for the synthesis of deuterium incorporated eugenols, such as deuterated eugenol (II), regioisomeric deuterated eugenol (III), and deuterated variant of methyl eugenol (V).

Facile Deoxygenation of Phenols and Enols Using Sodium Borohydride-Nickel Chloride

A facile deoxygenation reaction of phenol and 1,3-dicarbonyl compounds was investigated.Phenols, enolizable 1,3-diketones and 3-ketoesters were converted into the toluene-p-sulfonates which were reduced by a sodium borohydride-nickel chloride system to give the deoxygenated aromatic compounds, alcohols and esters, respectively.