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CAS 130304-80-2

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Fmoc-Asp(OcHex)-OH

Description:
Fmoc-Asp(OcHex)-OH, also known as Fmoc-protected aspartic acid with a hexyl ether side chain, is a chemical compound commonly used in peptide synthesis and research. The Fmoc (9-fluorenylmethoxycarbonyl) group serves as a protective group for the amino functionality, allowing for selective reactions during peptide assembly. The aspartic acid component contributes to the compound's acidic properties due to its carboxylic acid functional groups. The OcHex (octyl hexyl ether) moiety enhances the hydrophobic character of the molecule, which can influence solubility and interaction with other biomolecules. This compound is typically utilized in solid-phase peptide synthesis, where the Fmoc group can be removed under basic conditions, facilitating the sequential addition of amino acids. Its unique structure allows for the study of peptide behavior in various environments, making it valuable in biochemical and pharmaceutical research. Overall, Fmoc-Asp(OcHex)-OH is characterized by its protective Fmoc group, acidic aspartic acid core, and hydrophobic side chain, contributing to its utility in synthetic chemistry.
Formula:C25H27NO6
InChI:InChI=1/C25H27NO6/c27-23(28)14-22(24(29)32-16-8-2-1-3-9-16)26-25(30)31-15-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21/h4-7,10-13,16,21-22H,1-3,8-9,14-15H2,(H,26,30)(H,27,28)
SMILES:C1CCC(CC1)OC(=O)C(CC(=O)O)N=C(O)OCC1c2ccccc2c2ccccc12
Synonyms:
  • Fmoc-Asp(OcHx)-OH
  • Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 1-cyclohexyl ester
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