CAS 98628-27-4
:Boc-L-2-Amino-5-phenyl-pentanoic acid
Description:
Boc-L-2-Amino-5-phenyl-pentanoic acid, with the CAS number 98628-27-4, is a protected amino acid commonly used in peptide synthesis and medicinal chemistry. The "Boc" (tert-butyloxycarbonyl) group serves as a protective group for the amino function, allowing for selective reactions without interfering with the amine. This compound features a phenyl group attached to the pentanoic acid backbone, contributing to its hydrophobic characteristics, which can influence the solubility and biological activity of peptides synthesized from it. The presence of the amino group makes it a chiral molecule, which is significant in biological systems where chirality can affect the function and interaction of biomolecules. Boc-L-2-Amino-5-phenyl-pentanoic acid is typically utilized in the synthesis of more complex structures, including pharmaceuticals and biologically active compounds, due to its ability to facilitate the formation of peptide bonds. Its stability under standard laboratory conditions makes it a valuable intermediate in organic synthesis.
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Found 3 products.
Benzenepentanoic acid, a-[[(1,1-dimethylethoxy)carbonyl]amino]-, (S)-
CAS:Formula:C16H23NO4Purity:97%Color and Shape:SolidMolecular weight:293.3581(S)-2-((tert-Butoxycarbonyl)amino)-5-phenylpentanoic acid
CAS:(S)-2-((tert-Butoxycarbonyl)amino)-5-phenylpentanoic acidPurity:95%Molecular weight:293.36g/mol(S)-2-((tert-Butoxycarbonyl)amino)-5-phenylpentanoic acid
CAS:Formula:C16H23NO4Purity:97%Molecular weight:293.363



