88277-83-2

Usage

Uses

Used in Organic Synthesis:
C-[1,4]DIOXAN-2-YL-METHYLAMINE is used as a reagent in organic synthesis for its ability to participate in a variety of chemical reactions, facilitating the creation of new compounds with diverse properties. Its presence in the molecular structure allows for the formation of different functional groups, enhancing the reactivity and versatility of the synthesized products.
Used in Pharmaceutical Research:
In the pharmaceutical industry, C-[1,4]DIOXAN-2-YL-METHYLAMINE is utilized as an intermediate in the production of various drugs. Its unique structure contributes to the development of new medicinal compounds with potential therapeutic applications. Researchers leverage its properties to design and synthesize novel drug candidates, aiming to address unmet medical needs and improve treatment options for various diseases.
Used in Chemical Compound Development:
C-[1,4]DIOXAN-2-YL-METHYLAMINE is employed as a key component in the development of new chemical compounds with a broad spectrum of applications. Its integration into molecular structures allows for the exploration of new chemical spaces, leading to the discovery of innovative materials with unique properties and potential uses in various industries, including materials science, agrochemicals, and specialty chemicals.

InChI:InChI=1/C5H11NO2/c6-3-5-4-7-1-2-8-5/h5H,1-4,6H2

Upstream product

• 21048-16-8 2-(chloromethyl)-1,4-dioxane 
• 113019-61-7 2-Phthalimidomethyl-1,4-dioxane 

Downstream Products

• 113019-66-2 2-[([1,4]Dioxan-2-ylmethyl)-amino]-4-phenyl-thiazole-5-carboxylic acid ethyl ester 
• 1160507-04-9 5-(((1,4-dioxan-2-yl)methyl)(cyclohexylmethyl)amino)-1-methyl-3-propyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-one 
• 1442119-80-3 (±)-N-(1,4-dioxan-2-ylmethyl)-4-methyl-2-[(1-{4-[4-(trifluoromethyl)phenoxy]benzoyl}piperidin-4-yl)methyl]-2H-indazol-5-carboxamide 
• 1202699-94-2 N-[(1-[(2-chlorophenyl)methyl]-5-{[(1,4-dioxan-2-ylmethyl)amino]carbonyl}-4.6-dihydroxy-2-oxo-1,2-dihydro-3-pyridinyl)carbonyl]glycine 

Relevant academic research and scientific papers

Synthesis of mono- and bis(aminomethyl)dioxanes from N-[3-(2-chloroethoxy)-2-hydroxypropyl]sulfamates

N-Substituted aminomethyl- and 2,5-bis(aminomethyl)-1,4-dioxanes were prepared by cyclization of the corresponding potassium N-[3-(2-chloroethoxy)-2-hydroxypropyl]sulfamates under the action of an alkaline agent followed by alcoholysis of the resulting su