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CS-W001157 4
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(3S)Lenalidomide-5-methylpiperazine benzenesulfonate

  • CAS No. 2229714-16-1

  • Cat. No. CS-0198433
  • Purity≥95%
  • MDL No.None

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

(3S)Lenalidomide-5-methylpiperazine benzenesulfonate|CS-0198433

Structure of 2229714-16-1

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General Information

  • CAS No. 2229714-16-1
  • Cat. No. CS-0198433
  • Purity ≥95%
  • MDL No. None
  • Storage 4°C, sealed storage, away from moisture and light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₃H₂₆N₄O₆S
  • Molecular Weight 486.54
  • Synonym(s) None
  • SMILES S(=O)(=O)(O)C1=CC=CC=C1.O=C1N(CC=2C1=CC=C(C2)N3CCNCC3)[C@@H]4C(=O)NC(=O)CC4

Description

This bench-stable, moisture-tolerant piperidine-dione scaffold features a sterically hindered isoindolinone core paired with a piperazinyl substituent, enabling efficient integration into complex molecular architectures. The benzenesulfonate counterion enhances solubility and handling in synthetic workflows.

Application

(S)-3-(1-Oxo-5-(piperazin-1-yl)isoindolin-2-yl)piperidine-2,6-dione benzenesulfonate serves as a versatile intermediate in medicinal chemistry, enabling efficient construction of complex isoindolinone-based scaffolds. The piperazinyl substituent provides enhanced solubility and hydrogen-bonding capacity, while the benzenesulfonate counterion improves crystallinity and handling. It functions reliably in standard amide coupling and reductive amination workflows, offering high stability and compatibility with diverse functional groups under routine synthetic conditions.

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 : H315-H319
Precautionary Statements : P264-P280-P302+P352-P362

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Computational Chemistry Data

  • TPSA   81.75
  • LogP   -0.5355
  • H_Acceptors   7
  • H_Donors   2
  • Rotatable_Bonds   3

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