1191429-18-1

(R)-8-Azido-2-(Fmoc-amino)octanoic acid Chemical Structure
1191429-18-1

Chemical Structure

(R)-8-Azido-2-(Fmoc-amino)octanoic acid

  • CAS No.: 1191429-18-1
  • Formula:C23H26N4O4
  • Molecular Weight:422.48

IUPAC Name: (R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-8-azidooctanoic acid

InChIKey: ORGUFSNMGCTGEA-OAQYLSRUSA-N

SMILES: OC([C@@H](CCCCCCN=[N+]=[N-])NC(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O)=O

Biological Activity: (R)-8-Azido-2-(Fmoc-amino)octanoic acid is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1]. (R)-8-Azido-2-(Fmoc-amino)octanoic acid is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.

Cat. No. Product Name Purity Description Pricing
HY-131082
(R)-8-Azido-2-(Fmoc-amino)octanoic acid (R)-8-Azido-2-(Fmoc-amino)octanoic acid is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). (R)-8-Azido-2-(Fmoc-amino)octanoic acid is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
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