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CS-W001157 4
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Thalidomide-5-CH2-NH2 hydrochloride

  • CAS No. 1010100-22-7

  • Cat. No. CS-0187989
  • Purity≥98%
  • MDL No.MFCD32666042

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

Thalidomide-5-CH2-NH2 hydrochloride|CS-0187989

Structure of 1010100-22-7

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General Information

  • CAS No. 1010100-22-7
  • Cat. No. CS-0187989
  • Purity ≥98%
  • MDL No. MFCD32666042
  • Storage Store at room temperature, keep dry and cool
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₄H₁₄ClN₃O₄
  • Molecular Weight 323.73
  • Synonym(s) None
  • SMILES NCC1=CC(C(N(C2C(NC(CC2)=O)=O)C3=O)=O)=C3C=C1.Cl

Description

Thalidomide-5-CH2-NH2 (hydrochloride) features a primary amine handle at the 5-position, enabling site-specific conjugation in bioconjugate applications. This derivative maintains the core thalidomide scaffold while enhancing solubility and reactivity under physiological conditions. The hydrochloride salt improves stability and handling for bench-scale synthesis and medicinal chemistry workflows.

Application

Thalidomide-5-CH₂-NH₂ (hydrochloride) serves as a functionalized derivative of thalidomide, enabling targeted conjugation and scaffold modification in medicinal chemistry. The primary amine group facilitates efficient coupling reactions, while the hydrochloride salt enhances solubility and stability for handling. This compound functions as a key building block in the synthesis of analogs for targeted protein degradation and immunomodulatory drug discovery.

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

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Computational Chemistry Data

  • TPSA   109.57
  • LogP   -0.0317
  • H_Acceptors   5
  • H_Donors   2
  • Rotatable_Bonds   2

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