202923-63-5

Basic information

• Product Name: 2,5-Morpholinedione,3,6-dimethyl-,(3S)-(9CI)
• Synonyms: 2,5-Morpholinedione,3,6-dimethyl-,(3S)-(9CI)
• CAS NO: 202923-63-5
• Molecular Formula: C6H9NO3
• Molecular Weight: 143.14
• Product Categories: GLYCINESCAFFOLD
• Mol File: 202923-63-5.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,5-Morpholinedione,3,6-dimethyl-,(3S)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Morpholinedione,3,6-dimethyl-,(3S)-(9CI)(202923-63-5)
• EPA Substance Registry System: 2,5-Morpholinedione,3,6-dimethyl-,(3S)-(9CI)(202923-63-5)

Safety Data

• Hazardous Substances Data: 202923-63-5(Hazardous Substances Data)

Usage

Class

Cyclic imides

Appearance

White crystalline solid

Melting point

105-106°C

Potential applications

Chemistry and pharmaceuticals (as a starting material for the synthesis of various organic compounds)

Handling precautions

May pose risks if not used properly

Upstream product

• 56-41-7 L-alanin 
• 563-76-8 α-bromopropionyl bromide 
• 2491-20-5 L-alanine methyl ester hydrochloride 
• 409108-43-6 N-(2-hydroxypropionyl)alanine ethyl ester 
• 31654-38-3 N-(2-bromo-propionyl)-alanine 

Relevant articles and documents

Efficient synthesis of lactate-containing depsipeptides by the mitsunobu reaction of lactates

The Mitsunobu reaction has been used as an efficient tool for the synthesis of orthogonally-protected and unprotected depsipeptides such as Boc/Fmoc-L-Lys(Alloc)-D-Ala-D-Lac-OAllyl or L-Lys-D-Ala-D-Lac that are bacterial cell wall precursor analogues foun

Heterogeneous Catalytic Hydrogenation of Chiral Amino Acid Methyl Esters to Amino Alcohols with Retention of Configuration Over Mg-Modified Cu/ZnO/Al2O3 Catalyst

Selective hydrogenation of amino acid methyl esters to chiral amino alcohols is an important and fascinating process. The CuZn0.3Mg0.1AlOx catalyst for the synthesis of chiral amino alcohols was prepared by the fractional

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.

Process for the preparation of 3-, 6-substituted 2,5-morpholinediones

A process for the preparation of 3- and/or 6-substituted 2,5-morpholinediones is disclosed. Such morpholinediones are useful as precursors for the preparation of depsipeptide polymers and copolymers.