CAS 96314-26-0
:(4S)-4-Phenyl-L-proline
Description:
(4S)-4-Phenyl-L-proline is a chiral amino acid derivative characterized by its unique structure, which includes a proline backbone with a phenyl group attached to the fourth carbon. This compound is notable for its role in various biochemical processes and its applications in organic synthesis, particularly in the development of pharmaceuticals and as a building block in peptide synthesis. The presence of the phenyl group contributes to its hydrophobic characteristics, influencing its solubility and interaction with biological systems. As a chiral molecule, (4S)-4-Phenyl-L-proline can exist in two enantiomeric forms, but the (S)-enantiomer is often of particular interest due to its biological activity. This compound is typically white to off-white in appearance and is soluble in polar organic solvents. Its stereochemistry plays a crucial role in determining its reactivity and interaction with enzymes and receptors, making it a valuable compound in medicinal chemistry and drug design.
Formula:C11H13NO2
InChI:InChI=1S/C11H13NO2/c13-11(14)10-6-9(7-12-10)8-4-2-1-3-5-8/h1-5,9-10,12H,6-7H2,(H,13,14)/t9-,10+/m1/s1
InChI key:InChIKey=JHHOFXBPLJDHOR-ZJUUUORDSA-N
SMILES:C(O)(=O)[C@@H]1C[C@H](CN1)C2=CC=CC=C2
Synonyms:- (4S)-4-Phenyl-<span class="text-smallcaps">L</span>-proline
- 4-Phenyl-L-proline
- <span class="text-smallcaps">L</span>-Proline, 4-phenyl-, (4S)-
- <span class="text-smallcaps">L</span>-Proline, 4-phenyl-, trans-
- L-proline, 4-phenyl-
- Proline, 4-phenyl-
- trans-4-Phenyl-<span class="text-smallcaps">L</span>-proline
- trans-4-Phenyl-L-proline
- L-Proline, 4-phenyl-, (4S)-
- (4S)-4-Phenyl-L-proline
- L-Proline, 4-phenyl-, trans-
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Purity (%)
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100
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50
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90
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95
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100
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