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CS-W001157 4
Total: USD 88.00

1-Bromo-2-chloro-3,5-difluorobenzene

  • CAS No. 187929-82-4

  • Cat. No. CS-0028800
  • Purity≥98%
  • MDL No.MFCD00135441

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

1-Bromo-2-chloro-3,5-difluorobenzene|CS-0028800

Structure of 187929-82-4

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General Information

  • CAS No. 187929-82-4
  • Cat. No. CS-0028800
  • Purity ≥98%
  • MDL No. MFCD00135441
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₂BrClF₂
  • Molecular Weight 227.43
  • Synonym(s) None
  • SMILES FC1=CC(F)=C(Cl)C(Br)=C1

Description

1-Bromo-2-chloro-3,5-difluorobenzene is a halogenated aromatic compound featuring complementary reactive sites for cross-coupling transformations. The ortho-bromo and chloro substituents enable sequential functionalization, while the electron-deficient fluorine atoms enhance regioselectivity in palladium-catalyzed reactions. This bench-stable reagent integrates efficiently into complex molecular architectures under standard conditions.

Application

1-Bromo-2-chloro-3,5-difluorobenzene serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling palladium-catalyzed cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig arylations. Its orthogonal halogen reactivity profile—bromine for coupling, chlorine and fluorines for stability—facilitates selective functionalization. The compound exhibits excellent bench stability, ease of purification, and compatibility with diverse reaction conditions, making it ideal for constructing complex heterocyclic scaffolds and drug-like molecules.

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   3.3807
  • H_Acceptors   0
  • H_Donors   0
  • Rotatable_Bonds   0

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