Product Name:(R)-1-Methyl-5-oxopyrrolidine-2-carboxylic acid

IUPAC Name:(2R)-1-methyl-5-oxopyrrolidine-2-carboxylic acid

CAS:952345-00-5
Molecular Formula:C6H9NO3
Purity:97%
Catalog Number:CM255970
Molecular Weight:143.14

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CM255970-250mg in stock NJǤ
CM255970-1g in stock Ɠůʼn

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Product Details

CAS NO:952345-00-5
Molecular Formula:C6H9NO3
Melting Point:-
Smiles Code:O=C(O)[C@@H](CC1)N(C)C1=O
Density:
Catalog Number:CM255970
Molecular Weight:143.14
Boiling Point:
MDL No:MFCD26937700
Storage:Store at room temperature.

Category Infos

Amino Acids and Peptides
Amino acids are organic compounds containing a basic amino group and an acidic carboxyl group. Because amino acids contain both amino and carboxyl groups, they can be polymerized in an end-to-end manner, removing a molecule of water to form a covalent amide bond or peptide bond. Many amino acids are linked together end to end to form a polypeptide. Amino acids and peptides are important components in the fields of medicine and life sciences.
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Pyrrolidines
Pyrrolidine, also known as tetrahydropyrrole, is a saturated five-membered heterocyclic ring, which is miscible with water. Pyrrolidine exists in many alkaloids and drug molecules, such as kappa opioids, antagonists of dopamine D4 receptors, and HIV reverse transcriptase inhibitors.

Product Other Information

Product Overview (R)-1-Methyl-5-oxopyrrolidine-2-carboxylic acid, also known as MOPC-2, is a non-proteinogenic amino acid that has been used in a variety of scientific research applications. MOPC-2 is a chiral compound, meaning that it can exist in two mirror-image forms, and has been found to have a variety of biochemical and physiological effects. 
Synthesis Method (R)-1-methyl-5-oxopyrrolidine-2-carboxylic acid can be synthesized using a variety of methods. One of the most common methods is the reaction of 1-methyl-5-oxopyrrolidine-2-carboxaldehyde (MOPC-1) with hydrochloric acid in an aqueous solution. This reaction produces (R)-1-methyl-5-oxopyrrolidine-2-carboxylic acid and a byproduct of hydrochloric acid. Another method of synthesizing (R)-1-methyl-5-oxopyrrolidine-2-carboxylic acid is the reaction of 1-methyl-5-oxopyrrolidine-2-carboxylic acid (MOPC-3) with aqueous sodium hydroxide. This reaction produces (R)-1-methyl-5-oxopyrrolidine-2-carboxylic acid and a byproduct of sodium chloride.
Chemical Properties (R)-1-methyl-5-oxopyrrolidine-2-carboxylic acid is a relatively inexpensive compound, and it is relatively easy to synthesize.It has been found to be relatively stable and non-toxic, making it suitable for use in a variety of laboratory experiments.However, it has been found to be relatively slow-acting, meaning that it may take some time for its effects to be observed in laboratory experiments. Additionally, it has been found to be relatively unstable in acidic environments.
Synthesis and Application It has been used in the study of cell signaling pathways, as well as in studies of enzyme inhibitors, cancer therapeutics, and drug delivery systems. (R)-1-methyl-5-oxopyrrolidine-2-carboxylic acid has also been used to study the effects of oxidative stress on cells and to study the effects of environmental toxins on cells.
Future Directions These include further investigation into its effects on cell signaling pathways, its potential therapeutic applications, and its potential use as a drug delivery system. Additionally, further research into the synthesis of (R)-1-methyl-5-oxopyrrolidine-2-carboxylic acid and its stability in different environments could lead to more efficient and cost-effective production methods. Finally, further research into the biochemical and physiological effects of (R)-1-methyl-5-oxopyrrolidine-2-carboxylic acid could lead to a better understanding of its potential therapeutic applications.