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CS-W001157 4
Total: USD 88.00

1-Boc-3-piperidone

  • CAS No. 98977-36-7

  • Cat. No. CS-D0647
  • Purity≥95%
  • MDL No.MFCD01631193

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

1-Boc-3-piperidone|CS-D0647

Structure of 98977-36-7

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General Information

  • CAS No. 98977-36-7
  • Cat. No. CS-D0647
  • Purity ≥95%
  • MDL No. MFCD01631193
  • Storage -20°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₁₇NO₃
  • Molecular Weight 199.25
  • Synonym(s) None
  • SMILES O=C(N1CC(CCC1)=O)OC(C)(C)C

Description

1-Boc-3-piperidone features a protected piperidone core, enabling stable incorporation into complex molecular architectures. The Boc group ensures reliable deprotection under mild acidic conditions, facilitating downstream functionalization. This bench-stable reagent simplifies synthetic workflows in medicinal chemistry and peptide derivatization.

Synthesis

  • Route1

    References

    • COATS, STEVEN J.; BIAN, HAIYAN; CONNOLLY, PETER J.; BIGNAN, GILLES; CAI, CHAOZHONG; DAX, SCOTT L.; DECORTE, BART L.; LIN, SHU-CHEN; LIU, LI; MACIELAG, MARK J.; PITIS, PHILIP M.; ZHANG, YUE-MEI; ZHU, BIN; HE, WEI Patent: US2011/105520 A1, 2011 ; Location in patent: Page/Page column 36 ;
  • Route2
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      1-Boc-3-piperidone|CS-D0647
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    References

    • US2003/229094 A1, ; Page 123 ; US 20030229094 A1
  • Route3
    • null|null
      79-37-8
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      1-Boc-3-Hydroxypiperidine|CS-D0648
      85275-45-2
    • ~80%
    • In-stock
      1-Boc-3-piperidone|CS-D0647
      98977-36-7

    References

    • Kubo, Keiji; Miyawaki, Toshio; Kawamura, Masaki Patent: US2003/187023 A1, 2003 ;

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H319
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   46.61
  • LogP   1.5864
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   0

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