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Desamino lenalidomide-CH2NH2 hydrochloride

  • CAS No. 2248702-12-5

  • Cat. No. CS-0637628
  • Purity≥95%
  • MDL No.MFCD31746004

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

Desamino lenalidomide-CH2NH2 hydrochloride|CS-0637628

Structure of 2248702-12-5

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General Information

  • CAS No. 2248702-12-5
  • Cat. No. CS-0637628
  • Purity ≥95%
  • MDL No. MFCD31746004
  • Storage Store at room temperature, keep dry and cool
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₄H₁₆ClN₃O₃
  • Molecular Weight 309.75
  • Synonym(s) None
  • SMILES O=C1NC(C(CC1)N2C(C3=CC(CN)=CC=C3C2)=O)=O.Cl

Description

This piperidine-dione derivative features a strategically positioned aminomethyl group on the isoindolinone scaffold, enabling direct conjugation or functionalization. The hydrochloride salt enhances solubility and stability under standard conditions, facilitating use in synthetic workflows requiring precise amine handling.

Application

3-(6-(Aminomethyl)-1-oxoisoindolin-2-yl)piperidine-2,6-dione hydrochloride serves as a key heterocyclic building block for medicinal chemistry campaigns, enabling efficient access to isoindolinone-based scaffolds. The amine-functionalized side chain facilitates conjugation and derivatization, while the diketopiperazine core provides structural rigidity and enhanced metabolic stability. Bench-stable and compatible with standard purification methods, it functions effectively in peptide coupling, reductive amination, and macrocyclization 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

Quality Control

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Computational Chemistry Data

  • TPSA   92.5
  • LogP   -1.0561
  • H_Acceptors   6
  • H_Donors   2
  • Rotatable_Bonds   2

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