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CS-W001157 4
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4-Bromo-5-chloro-2-fluorobenzaldehyde

  • CAS No. 1603584-72-0

  • Cat. No. CS-0146391
  • Purity≥97%
  • MDL No.MFCD26142710

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

4-Bromo-5-chloro-2-fluorobenzaldehyde|CS-0146391

Structure of 1603584-72-0

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General Information

  • CAS No. 1603584-72-0
  • Cat. No. CS-0146391
  • Purity ≥97%
  • MDL No. MFCD26142710
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₃BrClFO
  • Molecular Weight 237.45
  • Synonym(s) None
  • SMILES O=CC1=CC(Cl)=C(Br)C=C1F

Description

4-Bromo-5-chloro-2-fluorobenzaldehyde features a trifluorinated aromatic core with strategically positioned halogens, enabling direct coupling in cross-coupling reactions. The aldehyde group provides a reactive handle for nucleophilic addition or condensation chemistry, while the electron-deficient ring enhances electrophilicity for downstream functionalization. This compound serves as a key building block in pharmaceutical intermediates and advanced materials synthesis.

Application

4-Bromo-5-chloro-2-fluorobenzaldehyde serves as a versatile electrophilic building block in medicinal chemistry and materials science, enabling direct incorporation of halogenated aromatic motifs into complex molecular architectures. Its trifunctional substitution pattern—bromine, chlorine, and fluorine—confers enhanced metabolic stability and modulates electronic properties, while the aldehyde group facilitates nucleophilic additions, imine formations, and downstream functionalization. Bench-stable and compatible with standard cross-coupling protocols (e.g., Suzuki, Stille), it functions efficiently in late-stage diversification and heterocycle 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   17.07
  • LogP   3.0541
  • H_Acceptors   1
  • H_Donors   0
  • Rotatable_Bonds   1

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