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CS-W001157 4
Total: USD 88.00

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
  • HazMat Fee +

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    The shipment is processed through FedEx Ground under the Limited Quantity option.

    Each bottle is packed as an Excepted Quantity, with a maximum of 1g for items in class 6.1 packing group I or II, and up to 25g for all other hazardous materials.

    If shipping is charged to your FedEx account, the HazMat fee will be billed directly by the courier. Otherwise, the fee will be included on your invoice. To help you avoid the HazMat fee, we can package a 5g order of a class 6.1 packing group I or II material as five separate 1g units, and a 100g order of any other dangerous good as four 25g units. This packaging adjustment will be made unless you instruct otherwise on your purchase order. Below, you will find the fee schedule from FedEx for handling hazardous materials.

    Type
    HazMat Fee
    Excepted Quantity $0.00
    FedEx Limited Quantities Ground $0.00
    Hazmat Ground shipping $50.00+
    Inaccessible (Haz class 6.1 or 9), Domestic $68.00+
    Accessible (Haz class 3, 4, 5 or 8), Domestic $158.00+
    Inaccessible (Haz class 6.1 or 9), International $108.00+
    Accessible (Haz class 3, 4, 5 or 8), International $238.00+

    An item is classified as a dangerous good if our website displays Hazardous Material (HazMat) information for it.

    There is a HazMat shipping fee for each item that qualifies as a dangerous good. Please contact our quotation team via email to confirm the details.

*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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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.

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

Computational Chemistry Data

  • TPSA   25.02
  • LogP   7.6803
  • H_Acceptors   1
  • H_Donors   1
  • Rotatable_Bonds   7

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-P330-P362+P364-P405-P501

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