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CS-W001157 4
Total: USD 88.00

Thalidomide-5-O-CH2-COOH

  • CAS No. 2467425-53-0

  • Cat. No. CS-0637358
  • Purity≥96%
  • MDL No.None

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

Thalidomide-5-O-CH2-COOH|CS-0637358

Structure of 2467425-53-0

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General Information

  • CAS No. 2467425-53-0
  • Cat. No. CS-0637358
  • Purity ≥96%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₅H₁₂N₂O₇
  • Molecular Weight 332.26
  • Synonym(s) None
  • SMILES O=C(O)COC1=CC2=C(C(N(C(CC3)C(NC3=O)=O)C2=O)=O)C=C1

Description

Thalidomide-5-O-CH2-COOH features a strategically positioned carboxymethyl ester at the 5-oxygen site, enhancing solubility and enabling bioorthogonal conjugation. This derivative retains the core phthalimide scaffold while introducing a reactive handle for peptide coupling or surface immobilization, facilitating targeted delivery applications in chemical biology and medicinal chemistry workflows.

Application

Thalidomide-5-O-CH₂-COOH serves as a functionalized derivative enabling targeted conjugation and prodrug strategies in medicinal chemistry. The pendant carboxylic acid group facilitates amide bond formation, esterification, or metal coordination, enhancing solubility and bioavailability. Its stability under standard reaction conditions supports reliable use in peptide coupling, antibody-drug conjugation, and scaffold diversification for immunomodulatory agents.

Safety Information

Download SDS
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-P305+P351+P338-P330-P362-P403+P233-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   130.08
  • LogP   -0.8306
  • H_Acceptors   9
  • H_Donors   2
  • Rotatable_Bonds   4

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