25306-99-4

Usage

Uses

Used in Specialty Chemicals Production:
Dimethyl (methoxymethyl)succinate serves as a key intermediate or starting material in the synthesis of specialty chemicals. Its unique properties and reactivity contribute to the development of a wide range of products in this industry.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, dimethyl (methoxymethyl)succinate is utilized as a solvent, intermediate, or starting material for the production of various pharmaceuticals. Its stability and low toxicity make it a preferred ingredient in controlled manufacturing settings.
Used in Solvent Applications:
Dimethyl (methoxymethyl)succinate is employed as a solvent in different industries due to its ability to dissolve a variety of substances. Its low toxicity and high stability make it a relatively safe option for use in controlled environments.

InChI:InChI=1/C8H14O5/c1-11-5-6(8(10)13-3)4-7(9)12-2/h6H,4-5H2,1-3H3

Upstream product

• 67-56-1 methanol 
• 81949-89-5 methoxymethyl-succinic acid 
• 617-54-9 citraconic acid dimethyl ester 
• 151-50-8 potassium cyanide 
• 124-41-4 sodium methylate 
• 617-52-7 Dimethyl itakonate 

Relevant academic research and scientific papers

Organocatalytic head-to-tail dimerization of methacrolein via conjugate addition of methanol: An alcohol activation mechanism proved by electrospray ionization mass spectrometry

The head-to-tail dimerization of methacrolein via the conjugate addition of methanol is catalyzed by various organic bases, such as an amine, phosphine, and N-heterocyclic carbene, to give 2,4-dimethyl-2-methoxymethylpentane-1,5-dial in moderate yields. Based on the interpretation of the key intermediates by electrospray ionization mass spectrometry, we propose a reaction mechanism involving the initial conjugate addition of the organic bases to methacrolein to generate a zwitterionic base followed by the activation of methanol.

2-Ethoxymethyl and 2-methoxymethyl N-(3,5-dichlorophenyl) succinamides

The invention relates to a selection of succinic acid imides that have, in the 2-position, alkoxy, alkoxyalkyl or acyloxy substituents having up to 4 carbon atoms and the imine components of which are derived from aliphatic amines having up to 5 carbon atoms or from aniline optionally having up to 2 substituents. The succinic acid imides according to the invention are used as fungicides. A method for their manufacture is also disclosed.