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CS-W001157 4
Total: USD 88.00

2-Chloro-4-fluorobromobenzene

  • CAS No. 110407-59-5

  • Cat. No. CS-W002418
  • Purity≥98%
  • MDL No.MFCD00142587

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

2-Chloro-4-fluorobromobenzene|CS-W002418

Structure of 110407-59-5

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General Information

  • CAS No. 110407-59-5
  • Cat. No. CS-W002418
  • Purity ≥98%
  • MDL No. MFCD00142587
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₃BrClF
  • Molecular Weight 209.44
  • Synonym(s) 4-Bromo-3-chlorofluorobenzene
  • SMILES BrC1=C(Cl)C=C(F)C=C1

Description

2-Chloro-4-fluorobromobenzene is a halogenated aromatic compound featuring complementary reactive sites for cross-coupling and functionalization. The ortho-chloro and para-fluoro substituents enable sequential transformations, while the bromine moiety serves as a robust handle for palladium-catalyzed coupling reactions under standard conditions. This molecule combines high stability with predictable reactivity, making it a reliable intermediate in synthetic sequences requiring precise regiocontrol.

Application

2-Chloro-4-fluorobromobenzene serves as a versatile building block in cross-coupling chemistry, enabling the construction of biaryl scaffolds via palladium-catalyzed reactions. Its orthogonal halogenation pattern facilitates sequential functionalization, while the bromine center offers high reactivity under standard Suzuki, Stille, and Negishi conditions. Bench-stable and amenable to purification by distillation or column chromatography, it supports efficient synthesis of complex aromatic architectures relevant to pharmaceutical and agrochemical research.

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

Quality Control

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Computational Chemistry Data

  • TPSA   0
  • LogP   3.2416
  • H_Acceptors   0
  • H_Donors   0
  • Rotatable_Bonds   0

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