CAS 72442-37-6
:1-methyl-5-oxo-DL-proline
Description:
1-Methyl-5-oxo-DL-proline, with the CAS number 72442-37-6, is an organic compound that belongs to the class of proline derivatives. It features a five-membered ring structure characteristic of proline, with a ketone functional group at the 5-position and a methyl group at the 1-position. This compound is typically a white to off-white solid and is soluble in polar solvents, which is common for many amino acid derivatives. The presence of the oxo group contributes to its reactivity, making it a potential intermediate in various synthetic pathways, particularly in the synthesis of peptides and other biologically active molecules. Its stereochemistry, being a DL-isomer, indicates the presence of both D- and L-forms, which can exhibit different biological activities. 1-Methyl-5-oxo-DL-proline may also play a role in metabolic processes and has potential applications in pharmaceuticals and biochemistry. However, detailed studies on its specific biological activities and applications are limited, necessitating further research for comprehensive understanding.
Formula:C6H9NO3
InChI:InChI=1/C6H9NO3/c1-7-4(6(9)10)2-3-5(7)8/h4H,2-3H2,1H3,(H,9,10)/t4-/m0/s1
InChI key:InChIKey=SHLYZEAOVWVTSW-UHFFFAOYSA-N
SMILES:C(O)(=O)C1N(C)C(=O)CC1
Synonyms:- 1-Methyl-5-oxo-<span class="text-smallcaps">DL</span>-proline
- 1-Methyl-5-oxoproline
- 1-Methyl-5-oxopyrrolidine-2-carboxylic acid
- 1-methyl-5-oxo-L-proline
- <span class="text-smallcaps">DL</span>-Proline, 1-methyl-5-oxo-
- Proline, 1-methyl-5-oxo-
- Pyroglutamic acid, 1-methyl-, <span class="text-smallcaps">DL</span>-
- Pyroglutamic acid, 1-methyl-, DL-
- 1-Methyl-5-oxo-DL-proline
- DL-Proline, 1-methyl-5-oxo-
- 1-Methyl-5-oxo-Proline
- N-methyl-2-pyrrolidone-5-carboxylic acid
- See more synonyms
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Found 4 products.
1-methyl-5-oxo-DL-proline
CAS:Formula:C6H9NO3Purity:97%Color and Shape:SolidMolecular weight:143.14061-Methyl-5-oxopyrrolidine-2-carboxylic acid
CAS:<p>1-Methyl-5-oxopyrrolidine-2-carboxylic acid is a pyroglutamate derivative that is synthesized by the reaction of methyllithium with a ketone. It is used as a reagent for the synthesis of esters and organolithium compounds. Racemization occurs when this compound reacts with an alcohol or phenol to form an ester or ether, respectively. The Grignard reagents are not reactive in the presence of air, but react readily in the presence of water or alcohol. Methyllithium (MeLi) and aryllithium (ArLi) are both organolithium reagents that react with alkyl halides to form organometallic compounds.</p>Formula:C6H9NO3Purity:Min. 95%Molecular weight:143.14 g/mol




