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CS-W001157 4
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3-Bromo-4,5-dihydroxybenzaldehyde

  • CAS No. 16414-34-9

  • Cat. No. CS-0103468
  • Purity≥95%
  • MDL No.MFCD00016608

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

3-Bromo-4,5-dihydroxybenzaldehyde|CS-0103468

Structure of 16414-34-9

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General Information

  • CAS No. 16414-34-9
  • Cat. No. CS-0103468
  • Purity ≥95%
  • MDL No. MFCD00016608
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₅BrO₃
  • Molecular Weight 217.02
  • Synonym(s) 5-BROMOPROTOCATECHUALDEHYDE
  • SMILES O=CC1=CC(O)=C(O)C(Br)=C1

Description

3-Bromo-4,5-dihydroxybenzaldehyde features a brominated aromatic ring flanked by two adjacent hydroxyl groups and a formyl functionality. This configuration enables direct incorporation into bioactive molecule scaffolds, particularly in the synthesis of catechol-containing pharmaceuticals and fluorescent probes. The compound exhibits enhanced reactivity in electrophilic substitution and transition-metal-catalyzed coupling reactions due to synergistic electronic effects from the electron-donating hydroxyls and the electron-withdrawing bromine.

Application

3-Bromo-4,5-dihydroxybenzaldehyde serves as a versatile building block for the synthesis of bioactive heterocycles and natural product analogs. The ortho-dihydroxy motif enables facile metal-catalyzed coupling reactions and oxidative cyclizations, while the bromine substituent provides a reliable handle for palladium-mediated cross-coupling. Its bench-stable crystalline form facilitates handling and purification, making it well-suited for iterative synthetic campaigns in medicinal chemistry and process development.

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   57.53
  • LogP   1.6728
  • H_Acceptors   3
  • H_Donors   2
  • Rotatable_Bonds   1

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