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tert-Butyl (9-hydroxynonyl)carbamate

  • CAS No. 1397043-36-5

  • Cat. No. CS-0433186
  • Molecule weight259.38
  • Purity≥95%
  • MDL No.MFCD02094529

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

tert-Butyl (9-hydroxynonyl)carbamate|CS-0433186

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General Information

  • CAS No. 1397043-36-5
  • Cat. No. CS-0433186
  • Purity ≥95%
  • MDL No. MFCD02094529
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₄H₂₉NO₃
  • Molecular Weight 259.38
  • Synonym(s) N-Boc-9-aminononan-1-ol
  • SMILES O=C(OC(C)(C)C)NCCCCCCCCCO

Description

tert-Butyl (9-hydroxynonyl)carbamate features a hydroxylated aliphatic chain appended to a robust tert-butyl carbamate protecting group, enabling selective conjugation and stability under standard conditions. This bifunctional scaffold integrates seamlessly into complex molecular architectures where controlled deprotection and site-specific derivatization are required.

Application

tert-Butyl (9-hydroxynonyl)carbamate serves as a stable, bench-friendly protecting group for primary amines, enabling selective functionalization in complex molecule synthesis. The hydroxyl group at the C9 position offers a handle for further derivatization, including oxidation to aldehydes or carboxylic acids, while the tert-butoxycarbonyl (Boc) moiety ensures compatibility with standard deprotection protocols. Its robustness under diverse reaction conditions facilitates efficient multistep syntheses.

Safety Information

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

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Computational Chemistry Data

  • TPSA   58.56
  • LogP   3.2341
  • H_Acceptors   3
  • H_Donors   2
  • Rotatable_Bonds   9

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