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CS-W001157 4
Total: USD 88.00

3-Bromo-5-iodobenzaldehyde

  • CAS No. 188813-09-4

  • Cat. No. CS-0186787
  • Purity≥98%
  • MDL No.None

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

3-Bromo-5-iodobenzaldehyde|CS-0186787

Structure of 188813-09-4

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General Information

  • CAS No. 188813-09-4
  • Cat. No. CS-0186787
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C, protect from light, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₄BrIO
  • Molecular Weight 310.91
  • Synonym(s) Benzaldehyde,3-bromo-5-iodo
  • SMILES C1=C(C=C(C=C1Br)I)C=O

Description

3-Bromo-5-iodobenzaldehyde features a dual-halogenated aromatic core with distinct reactivity at both bromine and iodine sites. The aldehyde group enables direct functionalization in cross-coupling and conjugation workflows. This electron-deficient scaffold integrates readily into complex molecular architectures under standard conditions, offering predictable regioselectivity in palladium-catalyzed transformations.

Application

3-Bromo-5-iodobenzaldehyde serves as a versatile bifunctional building block for cross-coupling cascades and sequential functionalization in medicinal chemistry. The aldehyde group enables direct derivatization via imine formation or reductive amination, while the bromo and iodo substituents support palladium-catalyzed coupling reactions with broad scope. Its bench-stable crystalline form facilitates handling and purification, making it ideal for constructing complex heterocyclic scaffolds and targeted API intermediates.

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   17.07
  • LogP   2.8662
  • H_Acceptors   1
  • H_Donors   0
  • Rotatable_Bonds   1

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