(2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone CAS: 945065-86-2
Catalog Number | XD93608 |
Product Name | (2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone |
CAS | 945065-86-2 |
Molecular Formula | C13H7ClFIO |
Molecular Weight | 360.55 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
(2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone is a chemical compound that belongs to the class of aryl ketones. Its molecular structure consists of a benzene ring with a chlorine atom at position 2, an iodine atom at position 5, and a fluorine atom at position 4, bonded to a carbonyl group (C=O) at the benzylic carbon. This compound has various applications in the field of organic synthesis and pharmaceutical research.One significant use of (2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone is as an intermediate in the synthesis of pharmaceutical compounds. The presence of different halogen atoms on the aromatic ring provides unique reactivity, allowing for further functionalization via substitution or coupling reactions. This compound can be utilized as a key starting material for the synthesis of diverse biologically active molecules, including drug candidates and pharmacologically active compounds.The halogen atoms, chlorine, iodine, and fluorine, present on the aromatic ring contribute to the compound's potential as a ligand in transition metal catalysis. The unique electronic properties of these halogens can facilitate the formation of coordination complexes when combined with metal catalysts. This can lead to the development of efficient and selective catalytic processes for the synthesis of complex organic molecules. These processes have broad applications in the pharmaceutical and fine chemical industries.Furthermore, (2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone can be utilized in the development of new materials. The combination of different halogens on the aromatic ring offers opportunities for chemical modifications, such as polymerization or copolymerization reactions. These modifications can lead to the creation of polymers with improved mechanical, thermal, or chemical properties. The resulting materials can find applications in various industries, including coatings, adhesives, and electronics.Additionally, this compound can be employed in the synthesis of fluorescent dyes and imaging agents. The distinct electronic properties of the halogens present in (2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone can enhance the fluorescence emission of dyes when incorporated into their molecular structure. This property makes these dyes suitable for use in biological imaging techniques, such as fluorescence microscopy or bioimaging assays.In conclusion, (2-Chloro-5-iodophenyl)(4-fluorophenyl)methanone is a versatile compound with applications in organic synthesis, pharmaceutical research, material science, and fluorescent imaging. Its unique molecular structure, incorporating different halogen atoms on the aromatic ring, provides opportunities for selective functionalization and the creation of valuable compounds. Further exploration of its applications may lead to the development of new pharmaceutical agents, advanced materials, or improved imaging techniques.