79494-95-4

Usage

Uses

Used in Organic Synthesis:
6-[(PhenylMethoxy)Methyl]-1,4-dioxane-2-Methanol is used as a key intermediate in the synthesis of various organic compounds for different industries. Its versatile structure enables it to act as a building block or a functional group in the creation of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 6-[(PhenylMethoxy)Methyl]-1,4-dioxane-2-Methanol is used as a starting material or an intermediate in the development of new drugs. Its ability to form a variety of chemical bonds and its compatibility with other molecules make it a valuable component in the synthesis of potential therapeutic agents.
Used in Agrochemical Industry:
6-[(PhenylMethoxy)Methyl]-1,4-dioxane-2-Methanol is also utilized in the agrochemical sector, where it serves as a precursor in the synthesis of pesticides, herbicides, and other crop protection agents. Its involvement in the development of these products helps to improve agricultural yields and ensure food security.
Used in Specialty Chemicals:
In the specialty chemicals market, 6-[(PhenylMethoxy)Methyl]-1,4-dioxane-2-Methanol is employed as a component in the production of various high-value chemicals. Its unique properties and reactivity contribute to the development of innovative materials and compounds for specific applications, such as in the fragrance, flavor, or dye industries.

Upstream product

• 338458-98-3 2-acetoxymethyl-6-benzyloxymethyl-1,4-dioxane 
• 100-51-6 benzyl alcohol 
• 338458-96-1 6-benzyloxymethyl-2-iodomethyl-1,4-dioxane 
• 83016-75-5 1-O-benzyl-3-O-allyl-1,2,3-propanetriol 
• 106-92-3 Allyl glycidyl ether 
• 338458-99-4 6-benzyloxymethyl-2-p-nitrobenzoyloxymethyl-1,4-dioxane 

Relevant academic research and scientific papers

Original synthesis of linear, branched and cyclic oligoglycerol standards

A variety of authentic standards of linear, branched and cyclic oligomers of glycerol, with well-defined structures and degrees of polymerisation from 2 to 5, have been efficiently synthesised. Linear oligomers were obtained by means of a convergent approach based on regioselective opening of bis(epoxides) with solketal; branched compounds were synthesised using oxidative cleavage of the corresponding anhydrohexitols as the key step. A 6-exo-trig halocyclisation reaction involving heteroatom-tethered unsaturated alcohols permitted an efficient synthesis of the precursors of selected cyclic dimers; larger cyclic oligomers were prepared by two one-pot Williamson reactions using a ditriflate derived from diglycerol. All these methodologies permitted further scaling up.

The reaction between epichlorohydrin and polysaccharides: Part 2, synthesis of some model substances, with cyclic substituents

Eight derivatives of methyl α-D-glucopyranoside, in which the substituents are part of cyclic structures, have been prepared as model substances for possible structural elements formed on reaction of polysaccharides with epichlorohydrin.The substances were converted into the permethylated alditol-1-d acetates and characterised by CIMS and EIMS. Keywords: Cross-linked polysaccharides; Epichlorohydrin

Anti-arrhythmia agents

Acetamide derivatives are provided having the structure STR1 wherein X is a single bond, --CH2 -- or --O--, R1 and R2 may be the same or different and are lower alkyl, phenyl-lower alkoxy-lower alkyl, lower alkenyl, phenyl-lower alkyl or lower alkoxy, or STR2 may be taken together to form a 5- to 7-membered heterocyclic ring optionally containing one other hetero atom, such as nitrogen, sulfur or oxygen; Y is hydroxyl, OR wherein R is lower alkyl, lower alkenyl or lower alkanoyl, or STR3 wherein R1 and R2, and R1 and R2 taken together with the nitrogen to which they are attached are as defined above, and n is 1 to 6. These compounds are useful as anti-arrhythmia agents and have been found to be effective in the treatment of acute myocardial infarction.