5129-78-2

Usage

Uses

Used in Organic Synthesis:
[formyl(methyl)amino]methyl benzoate is used as a key intermediate for the synthesis of various complex organic molecules. Its unique structure, which includes a formyl group, a methylamino group, and a benzoate group, allows for a range of reactions and the formation of diverse chemical products.
Used in Pharmaceutical Research:
In the pharmaceutical industry, [formyl(methyl)amino]methyl benzoate is used as a building block for the development of novel drugs. Its functional groups can be manipulated to create new molecules with potential therapeutic properties, contributing to the advancement of medical treatments.
Used in Chemical Compound Development:
[formyl(methyl)amino]methyl benzoate is employed as a starting material for the creation of new chemical compounds with specific applications. Its reactivity and structural diversity make it an attractive candidate for researchers looking to explore new chemical entities with potential uses in various industries.

Upstream product

• 123-39-7 N-Methylformamide 
• 50-00-0 formaldehyd 
• 98-88-4 benzoyl chloride 
• 20546-32-1 N-formyl-N-hydroxy-methyl-methylamine 
• 1854-28-0 benzoyloxy radical 
• 68-12-2 N,N-dimethyl-formamide 
• 65-85-0 benzoic acid 
• 611-73-4 Benzoylformic acid 

Relevant academic research and scientific papers

Bu4NI-catalyzed decarboxylative acyloxylation of an sp 3 C-H bond adjacent to a heteroatom with α-oxocarboxylic acids

A novel metal-free decarboxylative acyloxylation of an sp3 C-H bond in formamides and ethers has been explored. A variety of N-acyloxymethylamides and α-acyloxy ethers could be easily synthesized by this method. Preliminary mechanistic studies have shown that the reaction proceeded via a radical process. The Royal Society of Chemistry 2013.

Direct vs. Indirect Mechanisms in Organic Electrochemistry. Estimates of Activation Energies for Hydrogen Atom Transfer Processes of Relevance in Indirect Mechanisms Using the Bond Energy-Bond Order (BEBO) and Equibonding Methods

Activation energies for a number of hydrogen abstraction reactions of interest in mechanistic organic electrochemistry have been calculated using the bond energy-bond-order (BEBO) and equibonding method.The main emphasis has been put on processes with bearing on the problem of deciding between direct and indirect mechanisms in anodic oxidation, viz. acyloxylation, hydroxylation, methoxylation, nitrooxylation, cyanation, carbomethoxylation and azidation.The results indicate that indirect mechanisms might play a more important role than presently assumed.