4430-05-1

Usage

Uses

Used in Pharmaceutical Industry:
Morpholine-3,5-dione 97 is used as a building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs and improving the efficacy and safety of existing medications.
Used in Agrochemical Industry:
In the agrochemical industry, Morpholine-3,5-dione 97 is utilized as a building block for the synthesis of agrochemicals, helping to create more effective and environmentally friendly products for agricultural use.
Used in Organic Synthesis:
Morpholine-3,5-dione 97 is used as a reagent in organic synthesis, enabling the creation of a wide range of organic compounds for various applications, including the development of new materials and the improvement of existing ones.
Used in Polymer Production:
As a crosslinking agent, Morpholine-3,5-dione 97 is used in the production of polymeric materials, enhancing their properties and expanding their potential uses in various industries.

Upstream product

• 110-99-6 2,2'-oxybis-acetic acid 
• 4480-83-5 1,4-dioxane-2,6-dione 

Downstream Products

• 100461-08-3 4-Cyclohex-3-enylmethyl-morpholine-3,5-dione 
• 110-99-6 2,2'-oxybis-acetic acid 
• 1083088-18-9 4-(2-{4-[3-(3,4-dimethoxyphenyl)-4,4-dimethyl-5-oxo-4,5-dihydro-1H-pyrazol-1-yl]piperidin-1-yl}-2-oxoethyl)morpholine-3,5-dione 
• 500876-00-6 4-(2-{[5-Bromo-2-({3-chloro-4-[(2-methylphenyl)carbonyl]phenyl}amino)benzyl]oxy}ethyl)morpholine-3,5-dione 
• 22064-40-0 2-(2-amino-2-oxoethoxy)acetic acid 
• 24866-96-4 2-(4-chloro-benzyl)-morpholine-3,5-dione 
• 24866-95-3 2-benzyl-morpholine-3,5-dione 
• 24866-98-6 2-(hydroxy-diphenyl-methyl)-morpholine-3,5-dione 
• 24866-99-7 2-benzoyl-morpholine-3,5-dione 

Relevant academic research and scientific papers

Easy access to new heterocyclic systems: 1,4-Oxazine and substituted 1,4-oxazines

(Chemical Equation Presented) In the course of our investigations on the synthesis of new nitrogen heterocyclic derivatives, we were interested in the synthesis and study of new 1,4-oxazine rings. To this aim, the desired bisvinylphosphate was prepared fr

Synthesis and pyrolysis of tetrahydro-1,4-oxazine-3,5-diones and tetrahydro-1,4-thiazine-3,5-diones

The preparation and characterization of six 4-substituted tetrahydro-l,4-oxazine-3,5-diones and five 4-substituted tetrahydro-l,4-thiazine-3,5-diones is described. Upon flash vacuum pyrolysis at 700°C these give N-substituted acetamides and nitriles, and a mechanism for formation of these products is proposed.

Preparation of 2-(2-cyanoethyl)sulfanyl-1H-isoindole-1,3-(2H)-dione and related sulfur-transfer agents

The title compound 3 and 4-[(2-cyanoethyl)sulfanyl]morpholine-3,5-dione 12 are both conveniently prepared in good yield from 2-cyanoethyl disulfide, which itself is readily prepared in one step from S-(2-cyanoethyl)isothiouronium chloride 4. In the same way, dimethyl and diphenyl disulfides are converted, into 2-methylsulfanyl- and 2-phenylsulfanyl-1H-isoindole-1,3-(2H)-diones 8a and 8b, respectively, also in good yields.

CYCLISATIONS OF 1,3-THIAZINE-2,4-DIONES AND RELATED SYSTEMS

Thiazinediones 10 and 11 serve as starting materals for intramolecular amidoalkylations.While the stability of the derived hydroxy lactams 14 and 15 is lower as compared to carbocyclic analogs the ring closures to the bicyclic systems indicate a common order of reactivity of the corresponding N-acyliminium intermediate, e.g. 26.