CAS 2752-38-7
:N-Phenylacetyl-<span class="text-smallcaps">L</span>-proline
Description:
N-Phenylacetyl-L-proline, with the CAS number 2752-38-7, is an organic compound that belongs to the class of proline derivatives. It features a proline backbone, which is an amino acid known for its cyclic structure and role in protein synthesis. The compound is characterized by the presence of a phenylacetyl group attached to the nitrogen atom of the proline, which contributes to its unique properties. This modification can influence its solubility, stability, and biological activity. N-Phenylacetyl-L-proline is often studied for its potential applications in pharmaceuticals, particularly in the development of enzyme inhibitors and as a chiral auxiliary in asymmetric synthesis. Its structural characteristics may also impart specific interactions with biological targets, making it of interest in medicinal chemistry. Additionally, the compound may exhibit varying degrees of solubility in polar and non-polar solvents, which is essential for its application in different chemical environments. Overall, N-Phenylacetyl-L-proline is a compound of interest due to its structural features and potential utility in various chemical and biological contexts.
Formula:C13H15NO3
InChI:InChI=1S/C13H15NO3/c15-12(9-10-5-2-1-3-6-10)14-8-4-7-11(14)13(16)17/h1-3,5-6,11H,4,7-9H2,(H,16,17)/t11-/m0/s1
InChI key:InChIKey=UBQCWSGRNIOFFC-NSHDSACASA-N
SMILES:C(CC1=CC=CC=C1)(=O)N2[C@H](C(O)=O)CCC2
Synonyms:- L-Proline, 1-(phenylacetyl)-
- Proline, 1-(phenylacetyl)-, L-
- Proline, 1-(phenylacetyl)-
- L-proline, 1-(2-phenylacetyl)-
- 1-(2-Phenylacetyl)-L-proline
- L-Proline, 1-(2-phenylacetyl)-
- 1-(Phenylacetyl)-L-proline
- (S)-1-(2-phenylacetyl)pyrrolidine-2-carboxylic acid
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Found 2 products.
L-Proline, 1-(2-phenylacetyl)-
CAS:Formula:C13H15NO3Purity:97%Color and Shape:SolidMolecular weight:233.26311-(2-Phenylacetyl)pyrrolidine-2-carboxylic acid
CAS:<p>1-(2-Phenylacetyl)pyrrolidine-2-carboxylic acid is a synthetic acylase inhibitor. It is prepared from valine, chloroacetic acid, and phenylacetyl chloride by condensation of the carboxylic acid chloride with the amine in the presence of a base, followed by hydrolysis of the ester. 1-(2-Phenylacetyl)pyrrolidine-2-carboxylic acid can be used to prepare other compounds that have an acylase activity. This compound has been shown to inhibit acylases that are involved in reactions involving organic solvents or amino acids such as valine and methionine. The reaction rate for this compound is determined by its kinetic, which is stereospecific.</p>Formula:C13H15NO3Purity:Min. 95%Molecular weight:233.26 g/mol

