137032-88-3

Usage

Uses

Used in Pharmaceutical Industry:
2-(Methoxymethyl)-2-propenal serves as a chemical intermediate in the synthesis of pharmaceuticals, leveraging its reactivity to form complex molecules that can have therapeutic effects.
Used in Resin and Polymer Production:
In the chemical industry, 2-(Methoxymethyl)-2-propenal is utilized in the production of resins and polymers, contributing to the formation of durable and versatile materials for a wide range of applications.
Given the potential health hazards associated with 2-(Methoxymethyl)-2-propenal, it is crucial to implement proper safety measures and protective equipment when working with this chemical to minimize risks of irritation or other adverse effects.

InChI:InChI=1/C5H8O2/c1-5(3-6)4-7-2/h3H,1,4H2,2H3

Upstream product

• 137032-38-3 (2,2-Dimethoxy-1-methoxymethyl-1-methyl-ethylselanyl)-benzene 
• 21071-24-9 4-methoxybutanal 
• 111-92-2 dibutylamine 
• 107-02-8 acrolein 
• 14315-97-0 1,1,3-trimethoxypropane 
• 67-56-1 methanol 
• 50-00-0 formaldehyd 
• 137032-53-2 3-Methoxy-2-methyl-2-phenylselanyl-propionaldehyde 

Relevant academic research and scientific papers

SPIROINDOLINONE DERIVATIVES

The present invention relates to spiroindolinone derivatives of the formula and their enantiomers and pharmaceutically acceptable salts and esters thereof wherein R1, R2, R3, R4, R5, R6, R7 and R8, are as herein described.

Process for the manufacture of 2-alkoxymethylacrolein

There is provided a process for the manufacture of 2-alkoxymethylacrolein compounds via the reaction of an appropriate alcohol and acrolein in the presence of an acid and a trisubstituted amine to form an intermediate and the subsequent reaction of the intermediate with formaldehyde in the presence of an acid and a disubstituted amine. There is also provided a process for the manufacture of 3-alkoxymethylquinolines from 2-alkoxymethylacrolein.

Proccess for the manufacture of 2-alkoxymethylacrolein

There is provided a process for the manufacture of 2-alkoxymethylacrolein compounds via the reaction of an appropriate alcohol and acrolein in the presence of an acid and a trisubstituted amine to form an intermediate and the subsequent reaction of the intermediate with formaldehyde in the presence of an acid and a disubstituted amine.

Facile Access to 2-Alkylidene 3-Oxy Propanals and Propionic Acids from Conjugated Enals

Conjugated enals or their methyl acetals react with benzeneselenyl chloride in the presence of oxygen nucleophile to give Michael-type adducts.The latter are oxidized into 2-alkylidene 3-oxy propanals and propionic acids.