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CS-W001157 4
Total: USD 88.00

Thalidomide-5-Br

  • CAS No. 26166-92-7

  • Cat. No. CS-0080043
  • Purity≥95%
  • MDL No.MFCD30188073

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

Thalidomide-5-Br|CS-0080043

Structure of 26166-92-7

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General Information

  • CAS No. 26166-92-7
  • Cat. No. CS-0080043
  • Purity ≥95%
  • MDL No. MFCD30188073
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₃H₉BrN₂O₄
  • Molecular Weight None
  • Synonym(s) None
  • SMILES O=C1N(C(CC2)C(NC2=O)=O)C(C3=C1C=CC(Br)=C3)=O

Description

Thalidomide-5-Br features a bromine atom at the 5-position of the phthalimide ring, enhancing electrophilic reactivity for targeted conjugation. This derivative enables site-specific labeling in protein- and nucleic acid-based systems, leveraging its stable yet functionalized scaffold. Designed for chemical biology applications requiring controlled bioconjugation under physiological conditions.

Application

Thalidomide-5-Br serves as a brominated derivative of thalidomide, enabling site-specific functionalization in medicinal chemistry campaigns. The bromine substituent at the 5-position provides a handle for palladium-catalyzed cross-coupling reactions, facilitating the construction of diverse analogs and heterocyclic scaffolds. Its bench-stable solid form and established compatibility with standard synthetic protocols support efficient downstream derivatization in API research and target-oriented synthesis.

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+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   83.55
  • LogP   0.8346
  • H_Acceptors   6
  • H_Donors   1
  • Rotatable_Bonds   1

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