structure of BENZYL (2-BROMO-4-FORMYL-PHENYL) ETHER

BENZYL (2-BROMO-4-FORMYL-PHENYL) ETHER

CAS No.: 1000414-11-8
M. Wt: 277.11300
M. Fa: C13H9BrO2
InChI Key: -

Names and Identifiers of BENZYL (2-BROMO-4-FORMYL-PHENYL) ETHER

CAS Number

1000414-11-8

IUPAC Name

3-bromanyl-4-phenoxy-benzaldehyde

Canonical SMILES

C1=CC=C(C=C1)OC2=C(C=C(C=C2)C=O)Br

Physical and chemical properties of BENZYL (2-BROMO-4-FORMYL-PHENYL) ETHER

Exact Mass

275.97900

LogP

4.05390

Molecular Formula

C13H9BrO2

Molecular Weight

277.11300

PSA

26.30000

Applications of BENZYL (2-BROMO-4-FORMYL-PHENYL) ETHER

3-Bromo-4-phenoxybenzaldehyde has various applications:

  • Organic Synthesis: It serves as an intermediate in the synthesis of pharmaceuticals and agrochemicals.
  • Material Science: The compound can be used in developing new materials with specific properties due to its unique structural features.
  • Research Tool: Its reactivity makes it valuable in research settings for studying reaction mechanisms and developing new synthetic methodologies.

Interaction Studies of BENZYL (2-BROMO-4-FORMYL-PHENYL) ETHER

Interaction studies involving 3-bromo-4-phenoxybenzaldehyde focus on its reactivity with biological macromolecules and other small molecules. Research indicates that this compound can influence metabolic pathways by interacting with enzymes, potentially altering their activity or stability. Such interactions may provide insights into its pharmacological effects and help identify potential therapeutic applications.

Biological Activity of BENZYL (2-BROMO-4-FORMYL-PHENYL) ETHER

The biological activity of 3-bromo-4-phenoxybenzaldehyde is of interest due to its potential pharmacological properties. It has been reported to exhibit significant activity in biochemical pathways, influencing cellular processes such as apoptosis and oxidative stress responses. The compound's role as a reactant in synthesizing complex organic molecules suggests that it may interact with enzymes and proteins, facilitating various bio