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CS-W001157 4
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5-Bromo-3-(3-((tert-butyldiphenylsilyl)oxy)-2,2-dimethylpropyl)-2-iodo-1H-indole

  • CAS No. 2641451-43-4

  • Cat. No. CS-0433951
  • Purity≥97%
  • MDL No.None

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

5-Bromo-3-(3-((tert-butyldiphenylsilyl)oxy)-2,2-dimethylpropyl)-2-iodo-1H-indole|CS-0433951

Structure of 2641451-43-4

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General Information

  • CAS No. 2641451-43-4
  • Cat. No. CS-0433951
  • Purity ≥97%
  • MDL No. None
  • Storage -20°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₉H₃₃BrINOSi
  • Molecular Weight 646.47
  • Synonym(s) None
  • SMILES IC(N1)=C(CC(C)(C)CO[Si](C2=CC=CC=C2)(C(C)(C)C)C3=CC=CC=C3)C4=C1C=CC(Br)=C4

Description

This indole scaffold features a bromo substituent at C5 and an iodo group at C2, enabling sequential cross-coupling reactions. The tert-butyldiphenylsilyl-protected hydroxyl at the 3-position provides orthogonal reactivity and enhanced stability during multistep syntheses. This combination delivers a robust platform for constructing complex heterocyclic architectures in medicinal chemistry and natural product synthesis.

Application

5-Bromo-3-(3-((tert-butyldiphenylsilyl)oxy)-2,2-dimethylpropyl)-2-iodo-1H-indole serves as a versatile building block for the synthesis of complex indole-based scaffolds. The molecule combines a bromo- and iodo-substituted indole core with a silyl-protected hydroxyl group, enabling orthogonal functionalization in multi-step sequences. Its bench-stable nature and compatibility with palladium-catalyzed cross-coupling reactions facilitate efficient diversification in medicinal chemistry and natural product synthesis 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   25.02
  • LogP   7.6803
  • H_Acceptors   1
  • H_Donors   1
  • Rotatable_Bonds   7

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