CAS · 6630-33-7
Product Overview
2-Bromobenzaldehyde is a high-purity pharmaceutical-intermediates supplied for industrial and specialty chemical applications. Contact our team for specifications, packaging options and lead times.
Product Specifications
| Appearance | Pale yellow liquid or crystal |
|---|---|
| Purity (GC) | 99% min |
| Impurities (GC) | 1.0% max |
| Water (KF) | 0.2% max |
Applications
1. Pharmaceutical Intermediates
● Used in the synthesis of heterocycles, such as benzimidazoles, indoles, and quinolines, which form the backbone of many bioactive compounds.
● Essential for the production of:
Anti-inflammatory agents
Anticancer drugs
Antiviral and antibacterial compounds
2. Agrochemicals
● A starting material in the design of herbicides, fungicides, and insecticides.
● Enables the synthesis of halogenated aromatic compounds with pesticidal properties.
3. Ligand and Catalyst Development
● Functions as a precursor for synthesizing chelating ligands, especially Schiff bases, used in transition metal catalysis.
● Schiff bases derived from 2-bromobenzaldehyde show applications in asymmetric catalysis, coordination chemistry, and biomimetic systems.
4. Material Science
● Serves in the synthesis of fluorescent dyes, organic semiconductors, and photoactive compounds.
● The bromine atom allows further cross-coupling reactions for constructing π-conjugated systems in:
OLEDs
OFETs
Solar cells
5. Suzuki and Heck Coupling Reactions
● The aryl bromide group is reactive in palladium-catalyzed coupling reactions, enabling formation of complex aromatic systems.
● It can be selectively transformed while retaining the aldehyde for downstream modification.
Benefits
1. Dual Functional Reactivity
● The presence of both an aldehyde group (for condensation reactions) and a bromine substituent (for cross-coupling) makes it a highly flexible synthetic intermediate.
2. Positional Selectivity
● The ortho-substitution enhances regioselectivity in subsequent chemical transformations, allowing controlled synthesis of polysubstituted aromatics.
3. Facilitates Structural Diversification
● Acts as a scaffold for the synthesis of diverse molecular architectures through:
Reductive aminations
Grignard additions
Halogen–metal exchange reactions
4. Research Utility
● Frequently used in medicinal chemistry, natural product synthesis, and chemical biology studies.
● Well-characterized reactivity makes it a staple in academic and industrial R&D.
Conclusion
2-Bromobenzaldehyde丨CAS 6630-33-7 is a valuable compound in modern synthetic chemistry, offering dual-functionality that supports its use across pharmaceuticals, agrochemicals, catalysts, and advanced materials. Its ability to undergo diverse transformations makes it a preferred intermediate in both academic research and commercial production.
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