3,5-Dibromobenzaldehyde CAS: 56990-02-4
Catalog Number | XD94751 |
Product Name | 3,5-Dibromobenzaldehyde |
CAS | 56990-02-4 |
Molecular Formula | C7H4Br2O |
Molecular Weight | 263.91 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
3,5-Dibromobenzaldehyde is a compound that has various applications in different industries.
One of the main uses of 3,5-Dibromobenzaldehyde is as a building block in organic synthesis. It can be used as a starting material for the synthesis of various compounds, including pharmaceuticals, agrochemicals, and specialty chemicals. The dibromo substituents on the benzaldehyde ring enable the introduction of specific functionalities, allowing for the design of molecules with desired properties.
Furthermore, 3,5-Dibromobenzaldehyde finds application as a reagent in organic reactions. The dibromo group can undergo various transformations, such as substitution and coupling reactions, to form new carbon-carbon or carbon-heteroatom bonds. These reactions are essential in the synthesis of complex organic compounds, including natural products and drug candidates.
3,5-Dibromobenzaldehyde can also be used as a precursor in the production of dyes and pigments. It can undergo further functionalization reactions to introduce additional groups or undergo polymerization reactions to form polymeric dyes. These dyes and pigments have applications in various industries, including textiles, printing, and paints.
Moreover, 3,5-Dibromobenzaldehyde can find application as a reagent in analytical chemistry. It can react with various compounds to form colored products, which can be detected and quantified. This property makes 3,5-Dibromobenzaldehyde useful in assays and tests for the determination of certain analytes.
In addition, 3,5-Dibromobenzaldehyde can find application as a ligand in catalytic processes. The dibromo group can coordinate with transition metals, forming a complex that acts as a catalyst in various reactions. These reactions include cross-coupling reactions, hydrogenation, and other transformations. The presence of these functional groups can influence the selectivity and efficiency of the catalytic process.
In conclusion, 3,5-Dibromobenzaldehyde has versatile applications in organic synthesis, dye production, and catalysis. Its unique structure and properties make it a valuable compound in various industries, contributing to advancements in pharmaceuticals, materials science, and chemical research.