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CS-W001157 4
Total: USD 88.00

Desamino lenalidomide-NO2

  • CAS No. 1198787-23-3

  • Cat. No. CS-0614434
  • Purity≥97%
  • MDL No.MFCD33404278

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

Desamino lenalidomide-NO2|CS-0614434

Structure of 1198787-23-3

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General Information

  • CAS No. 1198787-23-3
  • Cat. No. CS-0614434
  • Purity ≥97%
  • MDL No. MFCD33404278
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₃H₁₁N₃O₅
  • Molecular Weight 289.24
  • Synonym(s) None
  • SMILES O=C1C2=CC=C([N+]([O-])=O)C=C2CN1C3C(NC(CC3)=O)=O

Description

This piperidine-2,6-dione scaffold features a 5-nitro-1-oxoisoindoline moiety that imparts strong electron-withdrawing character, enhancing reactivity in conjugate addition and cycloaddition processes. The fused ring system provides rigidity and defined spatial orientation, enabling precise molecular positioning in synthetic intermediates. Bench-stable under standard conditions, it integrates readily into complex heterocyclic architectures.

Application

3-(5-Nitro-1-oxoisoindolin-2-yl)piperidine-2,6-dione serves as a versatile scaffold for constructing bioactive heterocycles, leveraging the electron-deficient isoindolinone core and flanking diketone functionality. The nitro group enhances electrophilicity for nucleophilic addition, while the piperidinedione moiety provides a rigid, polar framework suitable for metal-catalyzed coupling and solid-phase synthesis. This compound enables efficient access to complex polycyclic systems under standard bench conditions, exhibiting robust stability and compatibility with common functional groups.

Safety Information

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Computational Chemistry Data

  • TPSA   112.3
  • LogP   -0.9826
  • H_Acceptors   7
  • H_Donors   1
  • Rotatable_Bonds   2

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