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CS-W001157 4
Total: USD 88.00

5-Bromo-1-chloro-3-fluoro-2-iodobenzene

  • CAS No. 83027-73-0

  • Cat. No. CS-0098780
  • Purity≥97%
  • MDL No.MFCD09878165

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

5-Bromo-1-chloro-3-fluoro-2-iodobenzene|CS-0098780

Structure of 83027-73-0

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General Information

  • CAS No. 83027-73-0
  • Cat. No. CS-0098780
  • Purity ≥97%
  • MDL No. MFCD09878165
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₂BrClFI
  • Molecular Weight None
  • Synonym(s) 1-Bromo-3-chloro-5-fluoro-4-iodobenzene
  • SMILES IC1=C(C=C(C=C1Cl)Br)F

Description

5-Bromo-1-chloro-3-fluoro-2-iodobenzene features a uniquely substituted aromatic core with halogens at every position, enabling precise functionalization in cross-coupling reactions. This electron-deficient scaffold integrates readily into complex molecular architectures under palladium-catalyzed conditions. The strategic placement of bromine, chlorine, fluorine, and iodine allows for sequential or selective transformations, streamlining access to diverse heterocyclic and biaryl frameworks in medicinal chemistry and materials science.

Application

5-Bromo-1-chloro-3-fluoro-2-iodobenzene serves as a versatile multi-heteroaryl building block for palladium-catalyzed cross-coupling reactions. Its orthogonal halogen reactivity enables sequential functionalization, while the fluorine substituent enhances metabolic stability and modulates electronic properties in target scaffolds. Bench-stable and compatible with standard coupling conditions, it facilitates efficient access to complex substituted arenes used in pharmaceutical and agrochemical synthesis.

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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   0
  • LogP   3.8462
  • H_Acceptors   0
  • H_Donors   0
  • Rotatable_Bonds   0

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