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CS-W001157 4
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tert-Butyl non-8-yn-1-ylcarbamate

  • CAS No. 1903797-81-8

  • Cat. No. CS-0636320
  • Purity≥95%
  • MDL No.None

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

tert-Butyl non-8-yn-1-ylcarbamate|CS-0636320

Structure of 1903797-81-8

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General Information

  • CAS No. 1903797-81-8
  • Cat. No. CS-0636320
  • Purity ≥95%
  • MDL No. None
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₄H₂₅NO₂
  • Molecular Weight 239.35
  • Synonym(s) None
  • SMILES O=C(OC(C)(C)C)NCCCCCCCC#C

Description

tert-Butyl non-8-yn-1-ylcarbamate features a terminal alkyne group flanked by a sterically hindered tert-butyl carbamate protecting group. This combination enables stable incorporation of the alkyne into synthetic sequences, facilitating efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC) and other click chemistry applications under standard conditions.

Application

tert-Butyl non-8-yn-1-ylcarbamate serves as a versatile, bench-stable building block for the synthesis of alkyne-functionalized amine derivatives. Its terminal alkyne group enables reliable copper-catalyzed azide-alkyne cycloaddition (CuAAC), while the tert-butoxycarbonyl (Boc) group provides orthogonal protection for primary amines. The molecule exhibits excellent functional group tolerance and facilitates straightforward purification, making it ideal for modular peptide and heterocyclic scaffold construction in medicinal chemistry workflows.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   38.33
  • LogP   3.4849
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   7

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