AE22395
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Catalog Number: | AE22395 |
Chemical Name: | 2-(2,6-Difluorophenyl)acetaldehyde |
CAS Number: | 109346-83-0 |
Molecular Formula: | C8H6F2O |
Molecular Weight: | 156.1294 |
MDL Number: | MFCD11110139 |
SMILES: | O=CCc1c(F)cccc1F |
2-(2,6-Difluorophenyl)acetaldehyde is a crucial compound utilized in organic chemical synthesis for its unique properties and versatility. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Known for its aromatic nature and electron-withdrawing difluoromethyl groups, 2-(2,6-Difluorophenyl)acetaldehyde plays a significant role in the development of complex molecular structures.In chemical synthesis, 2-(2,6-Difluorophenyl)acetaldehyde acts as a key intermediate in the construction of diverse organic molecules. Its reactive aldehyde group can undergo various transformations, such as condensation reactions, nucleophilic additions, and reduction processes, to form new carbon-carbon or carbon-heteroatom bonds. This enables the synthesis of a wide range of compounds with tailored structures and functionalities.Moreover, the difluorophenyl moiety in 2-(2,6-Difluorophenyl)acetaldehyde imparts unique physicochemical properties to the resulting molecules, enhancing their biological activity, stability, or other desirable characteristics. By incorporating this specific functional group into target molecules, researchers can modulate their properties for specific applications in the fields of medicine, agriculture, or materials science.Overall, 2-(2,6-Difluorophenyl)acetaldehyde proves to be a valuable tool in the hands of synthetic chemists, offering a platform for the efficient and strategic synthesis of diverse chemical compounds with enhanced properties and applications in various industries.