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CAS 13798-75-9

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BOC-ASP(OBZL)-OSU

Description:
BOC-ASP(OBZL)-OSU, with the CAS number 13798-75-9, is a chemical compound that serves as a derivative of aspartic acid, often utilized in peptide synthesis and bioconjugation applications. The "BOC" (tert-butyloxycarbonyl) group is a common protecting group for amines, which helps to prevent unwanted reactions during synthesis. The "OBZL" (benzyl) group is another protecting moiety that can be removed under specific conditions, allowing for selective deprotection of functional groups. The "OSU" (N-hydroxysuccinimide ester) component is particularly important for facilitating the formation of amide bonds with nucleophiles, such as amino groups in peptides or proteins. This compound is typically used in research and development settings, particularly in the fields of medicinal chemistry and biochemistry, where it aids in the synthesis of complex molecules. Its stability, reactivity, and ability to selectively protect functional groups make it a valuable tool in organic synthesis and peptide chemistry.
Formula:C20H24N2O8
InChI:InChI=1/C20H24N2O8/c1-20(2,3)29-19(27)21-14(18(26)30-22-15(23)9-10-16(22)24)11-17(25)28-12-13-7-5-4-6-8-13/h4-8,14H,9-12H2,1-3H3,(H,21,27)
SMILES:CC(C)(C)OC(=NC(CC(=O)OCc1ccccc1)C(=O)ON1C(=O)CCC1=O)O
Synonyms:
  • Boc-L-Aspartic Acid 4-Benzyl 1-(Hydroxysuccinimide) Ester
  • Boc-L-Aspartic Acid Beta-Bensyl Ester N-Hydroxysuccinimide Ester
  • Boc-L-Aspartic Acid-Beta-Benzyl-Alpha-Hydroxysuccinimide Ester
  • Boc-L-Aspartic Acid Beta-Benzyl-Alpha-N-Hydroxysuccinimide Di-Ester
  • Boc-L-Aspartic Acid Beta-Benzyl-Hydroxysuccinimide Ester
  • Boc-Aspartic Acid(Obzl)-Osu
  • N-Alpha-T-Boc-L-Aspartic Acid Beta-Benzyl Ester N-Hydroxysuccinimide Ester
  • 4-benzyl 1-(2,5-dioxopyrrolidin-1-yl) N-(tert-butoxycarbonyl)aspartate
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