71155-68-5

Usage

Uses

Used in Pharmaceutical Synthesis:
[3-(acetyloxy)-4-methoxyphenyl]methanediyl diacetate is used as an intermediate in the synthesis of pharmaceuticals and natural products. Its versatile chemical structure allows for the creation of various compounds with potential therapeutic applications.
Used in Research and Development:
In the research industry, [3-(acetyloxy)-4-methoxyphenyl]methanediyl diacetate is used as a key compound in the development of new drugs and therapies. Its anti-inflammatory and antioxidant properties make it a promising candidate for further study and potential applications in the treatment of various diseases.
Used in Anti-inflammatory Applications:
[3-(acetyloxy)-4-methoxyphenyl]methanediyl diacetate is used as an anti-inflammatory agent for its potential to alleviate inflammation and reduce the associated pain and swelling. This application is particularly relevant in the development of treatments for conditions such as arthritis and other inflammatory disorders.
Used in Antioxidant Applications:
As an antioxidant agent, [3-(acetyloxy)-4-methoxyphenyl]methanediyl diacetate is used to protect cells from damage caused by free radicals and oxidative stress. This property makes it a valuable compound in the development of treatments for diseases associated with oxidative stress, such as cardiovascular disorders and certain types of cancer.
Used in Cancer Treatment Research:
[3-(acetyloxy)-4-methoxyphenyl]methanediyl diacetate is used as a compound in the research and development of potential cancer treatments. Its potential anti-inflammatory and antioxidant properties may contribute to the development of therapies that target cancer cells while minimizing damage to healthy cells.

Upstream product

• 621-59-0 isovanillin 
• 108-24-7 acetic anhydride 

Downstream Products

• 881-57-2 isovanillin acetate 

Relevant academic research and scientific papers

SiO2@FeSO4 nano composite as nanocatalyst for the green synthesis 1,1-diacetates from aldehydes under solvent-free conditions

Aldehydes compounds selective converted to 1,1-diacetates as protective reagent with SiO2@FeSO4 nano composite as effective nano catalyst at room temperature under solvent-free condition and acetic anhydride (Ac2O) as acet

An efficient method for the synthesis of acylals from aldehydes under solvent-free conditions catalyzed by antimony trichloride

A mild and efficient method has been developed for the preparation of acylals from aldehydes catalyzed by antimony trichloride under solvent-free conditions in very good to excellent yields. The easy availability, low cost, and ease of handling of the catalyst make this procedure especially attractive for large-scale synthesis. Copyright Taylor & Francis Group, LLC.

Cobalt(II)-Catalyzed Reaction of Aldehydes with Acetic Anhydride under an Oxygen Atmosphere: Scope and Mechanism

The reaction of aldehydes with acetic anhydride in the presence of catalytic cobalt(II) chloride under an oxygen atmosphere at ambient temperature is dependent upon the reaction medium.Aliphatic aldehydes react in acetonitrile to give 1,2-diones whereas the aromatic aldehydes are acylated to yield the corresponding acylals.On the other hand, carboxylic acids are obtained from aliphatic and aromatic aldehydes by conducting the reaction in dichloroethane or benzene.Cobalt(II) chloride in acetonitrile catalyzes the conversion of aliphatic aldehydes to the correspondinganhydrides in the absence of acetic anhydride whereas aromatic aldehydes remain largely unaffected under these conditions.A preliminary mechanistic study in three different solvents (i.e. acetonitrile, dichloroethane, and DMF) has revealed that in acetonitrile and in the presence of acetic anhydride, aliphatic aldehydes behave differently than aromatic aldehydes.Some trapping experiments using methyl acrylate and stilbene have been conducted to demonstrate the occurence of an acyl cobalt and peroxyacyl cobalt intermediate during these reactions.