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CS-W001157 4
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3-Bromo-2-chlorobenzaldehyde

  • CAS No. 1197050-28-4

  • Cat. No. CS-0094382
  • Purity≥98%
  • MDL No.MFCD12024585

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

3-Bromo-2-chlorobenzaldehyde|CS-0094382

Structure of 1197050-28-4

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General Information

  • CAS No. 1197050-28-4
  • Cat. No. CS-0094382
  • Purity ≥98%
  • MDL No. MFCD12024585
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₄BrClO
  • Molecular Weight 219.46
  • Synonym(s) 3-broMo-2-chloro benzaldehyde
  • SMILES O=CC1=CC=CC(Br)=C1Cl

Description

3-Bromo-2-chlorobenzaldehyde features a sterically constrained aromatic core with complementary halogen substituents, enabling selective cross-coupling reactions. The aldehyde group provides a reactive handle for nucleophilic additions and condensation chemistry under standard conditions. This molecule integrates seamlessly into complex synthetic sequences requiring precise functional group placement.

Application

3-Bromo-2-chlorobenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The aldehyde functionality facilitates downstream transformations such as reductive amination and Wittig olefination, while the bromo and chloro substituents offer complementary sites for selective functionalization. Bench-stable and readily purified by distillation, it functions effectively in multi-step syntheses requiring precise regiocontrol.

Safety Information

Download SDS
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   2.915
  • H_Acceptors   1
  • H_Donors   0
  • Rotatable_Bonds   1

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