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Fmoc-S-3-amino-5-hexynic acid

  • CAS No. 1217669-02-7

  • Cat. No. CS-0182726
  • Molecule weight349.38
  • Purity≥95%
  • MDL No.MFCD01861008

*For research and further manufacturing use only, not for direct human use.

Fmoc-S-3-amino-5-hexynic acid|CS-0182726

Structure of 1217669-02-7

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General Information

  • CAS No. 1217669-02-7
  • Cat. No. CS-0182726
  • Purity ≥95%
  • MDL No. MFCD01861008
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₁H₁₉NO₄
  • Molecular Weight 349.38
  • Synonym(s) FMoc-(S)-3-AMino-5-hexynoic acid
  • SMILES C#CC[C@H](NC(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O)CC(O)=O

Description

Fmoc-S-3-amino-5-hexynic acid integrates a terminal alkyne and primary amine for bioorthogonal conjugation. This bifunctional reagent enables site-specific labeling via CuAAC or strain-promoted reactions, combining high reactivity with stability under standard conditions. The Fmoc group facilitates efficient solid-phase synthesis and protection of the amine.

Application

Fmoc-S-3-amino-5-hexynic acid serves as a versatile building block for the synthesis of peptidomimetics and bioconjugates. Its terminal alkyne enables efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC), while the Fmoc-protected amine and carboxylic acid facilitate standard solid-phase peptide synthesis. The molecule exhibits excellent bench stability, ease of purification, and compatibility with diverse functional groups, making it ideal for constructing complex scaffolds in medicinal chemistry and chemical biology workflows.

Safety Information

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GHS Pictogram :
GHS No : GHS06
Signal Word : Danger
UN#: 2811
Class : 6.1
Packing Group : Ⅲ
Hazard Statements : H301
Precautionary Statements : P264-P270-P330-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   75.63
  • LogP   3.3917
  • H_Acceptors   3
  • H_Donors   2
  • Rotatable_Bonds   6

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