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CAS 4530-18-1

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Boc-DL-Phe-OH

Description:
Boc-DL-Phe-OH, or N-tert-butoxycarbonyl-DL-phenylalanine, is a derivative of the amino acid phenylalanine, characterized by the presence of a tert-butoxycarbonyl (Boc) protecting group on the amino group. This compound is typically utilized in peptide synthesis as a protective group that facilitates the selective modification of amino acids. The Boc group is stable under basic conditions but can be removed under acidic conditions, allowing for the regeneration of the free amine. Boc-DL-Phe-OH is a white to off-white crystalline solid, and it is soluble in organic solvents such as dichloromethane and dimethylformamide, but less soluble in water. Its molecular structure includes a phenyl ring, contributing to its hydrophobic characteristics, which can influence its interactions in biological systems. The compound is often used in research and pharmaceutical applications, particularly in the synthesis of peptides and other bioactive molecules. Safety data should be consulted for handling, as with all chemical substances, to ensure proper laboratory practices.
Formula:C15H21NO4
InChI:InChI=1/C15H21NO4/c1-15(2,3)20-14(19)16(4)12(13(17)18)10-11-8-6-5-7-9-11/h5-9,12H,10H2,1-4H3,(H,17,18)
SMILES:CC(C)(C)OC(=O)N(C)C(Cc1ccccc1)C(=O)O
Synonyms:
  • N-(tert-butoxycarbonyl)-N-methylphenylalanine
  • Boc-DL-phenylalanine
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