118363-62-5

Basic information

• Product Name: 2,5-Morpholinedione,3,6-dimethyl-(9CI)
• Synonyms: 2,5-Morpholinedione,3,6-dimethyl-(9CI)
• CAS NO: 118363-62-5
• Molecular Formula: C6H9NO3
• Molecular Weight: 143.14056
• Product Categories: GLYCINESCAFFOLD
• Mol File: 118363-62-5.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,5-Morpholinedione,3,6-dimethyl-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Morpholinedione,3,6-dimethyl-(9CI)(118363-62-5)
• EPA Substance Registry System: 2,5-Morpholinedione,3,6-dimethyl-(9CI)(118363-62-5)

Safety Data

• Hazardous Substances Data: 118363-62-5(Hazardous Substances Data)

Usage

Also known as

3,6-dimethyl-2,5-morpholinedione

Class

Substituted morpholine-2,5-diones

Structure

Cyclic amide derivative with a morpholine ring and two methyl groups attached at the 3 and 6 positions

Physical form

White crystalline solid

Solubility

Soluble in water and organic solvents

Applications

Organic synthesis, pharmaceuticals, agricultural products, building block in the production of various compounds

Safety precautions

Proper handling and safety precautions should be observed when working with this chemical.

Upstream product

• 409108-43-6 N-(2-hydroxypropionyl)alanine ethyl ester 
• 31654-38-3 N-(2-bromo-propionyl)-alanine 

Relevant articles and documents

Biodegradable bio-absorbable material for clinical practice and method for producing the same

Bio-absorbable polymers such as vascular stent and suture thread for use as materials for clinical practice have almost definite dynamic properties such as tensile strength and degradation rate for absorption. When the dynamic properties thereof are elevated, therefore, the bio-absorbable polymers turn fragile, involving slower degradation rate. When the degradation rate is elevated, further, the dynamic properties are deteriorated. Disadvantageously, such bio-absorbable polymers have limited purposes for use and limited sites for use. Thus, copolymerization of bio-absorbable polymers with a cyclic depsipeptide to form a copolymer of the ring-opened and copolymerized depsipeptide can allow the adjustment of the dynamic properties and degradation rate of the resulting copolymer depending on the content of the depsipeptide.