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CAS 179412-79-4

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BOC-D-LEU-OH

Description:
BOC-D-LEU-OH, also known as Boc-D-leucine, is a chemical compound characterized by its structure as a derivative of the amino acid leucine. It features a tert-butyloxycarbonyl (Boc) protecting group, which is commonly used in peptide synthesis to protect the amino group of the amino acid. This compound is typically a white to off-white solid and is soluble in organic solvents such as methanol and dimethyl sulfoxide (DMSO), but has limited solubility in water. BOC-D-LEU-OH is primarily utilized in the field of organic chemistry and biochemistry for the synthesis of peptides and other complex molecules, allowing for the selective modification of amino acids. Its stability under various conditions makes it a valuable intermediate in synthetic pathways. Additionally, the presence of the Boc group facilitates the deprotection process, enabling the release of the free amino group when needed. Overall, BOC-D-LEU-OH is an important reagent in peptide chemistry and related applications.
Formula:C11H21NO4
Synonyms:
  • (S)-3-(Boc-Amino)-4-Methylpentanoic Acid
  • (S)-3-(Boc-amino)-4-methylpentanoic acid, Boc-D-β-Homoval-OH, Boc-D-β-Leucine
  • (S)-3-[(tert-butoxycarbonyl)amino]-4-methylpentanoic acid
  • (3S)-3-{[(tert-butoxy)carbonyl]amino}-4-methylpentanoic acid
  • Pentanoic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-methyl-, (3S)-
  • Boc-D-beta-Leucine
  • (Tert-Butoxy)Carbonyl D-β-homovaline
  • Boc-D-p-HomoValine
  • Boc-D-beta-HomoVal-OH
  • Boc-D-β-Homo-Val-OH
  • Boc-D-β-homovaline
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