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CAS 73259-81-1

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N(alpha)-boc-L-2,3-diaminopropionic acid

Description:
N(alpha)-Boc-L-2,3-diaminopropionic acid is a protected form of the amino acid 2,3-diaminopropionic acid, which is notable for its role in peptide synthesis and as a building block in the development of various pharmaceuticals. The "Boc" (tert-butyloxycarbonyl) group serves as a protective group for the amino functionality, enhancing the stability and solubility of the compound during chemical reactions. This substance typically appears as a white to off-white crystalline solid and is soluble in polar organic solvents. Its molecular structure features two amine groups, which can participate in various chemical reactions, making it versatile in synthetic chemistry. The compound is often used in the synthesis of peptides and other complex molecules due to its ability to facilitate the formation of peptide bonds. Additionally, it may exhibit biological activity, although specific biological properties would depend on the context of its use. Proper handling and storage conditions are essential to maintain its integrity and reactivity in laboratory settings.
Formula:C8H16N2O4
InChI:InChI=1/C8H16N2O4/c1-8(2,3)14-7(13)10-5(4-9)6(11)12/h5H,4,9H2,1-3H3,(H,10,13)(H,11,12)/t5-/m0/s1
SMILES:CC(C)(C)OC(=N[C@@H](CN)C(=O)O)O
Synonyms:
  • Boc-Dap-OH
  • Boc-Dpr-OH, N-Boc-L-2,3-diaminopropanoic acid
  • Na-Boc-L-2,3-diaminopropionic acid
  • N-t-BOC--amino-L-alanine
  • Boc-Dap
  • 3-amino-N-(tert-butoxycarbonyl)-L-alanine
  • N-alpha-L-(Butoxycarbonyl)-2,3-diaminopropionic acid
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