CAS 13500-55-5
:L-Proline, 4-ethoxy-, trans-
Description:
L-Proline, 4-ethoxy-, trans- is an amino acid derivative characterized by its unique structure, which includes a proline backbone with an ethoxy group at the fourth position. This compound is a chiral molecule, meaning it exists in two enantiomeric forms, although the trans configuration is specifically noted. L-Proline itself is a non-essential amino acid that plays a crucial role in protein synthesis and is involved in various metabolic processes. The ethoxy substitution can influence the compound's solubility, reactivity, and interaction with biological systems. Typically, such derivatives may exhibit specific biological activities, potentially affecting their use in pharmaceuticals or as biochemical tools. The presence of the ethoxy group may enhance lipophilicity, impacting the compound's pharmacokinetics. Overall, L-Proline, 4-ethoxy-, trans- is of interest in both synthetic chemistry and biochemistry, particularly in the context of drug design and development.
Formula:C7H13NO3
InChI:InChI=1S/C7H13NO3/c1-2-11-5-3-6(7(9)10)8-4-5/h5-6,8H,2-4H2,1H3,(H,9,10)/t5-,6+/m1/s1
InChI key:InChIKey=UGNGLHKEESUVLW-RITPCOANSA-N
SMILES:C(O)(=O)[C@@H]1C[C@@H](OCC)CN1
Synonyms:- Proline, 4-ethoxy-, L-trans-
- L-Proline, 4-ethoxy-, trans-
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