4-Bromo-2-methylthiophene CAS:29421-92-9
Catalog Number | XD96167 |
Product Name | 4-Bromo-2-methylthiophene |
CAS | 29421-92-9 |
Molecular Formula | C5H5BrS |
Molecular Weight | 177.06 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
4-Bromo-2-methylthiophene is an organobromine compound that contains a bromine atom attached to a thiophene ring. Thiophene derivatives are widely used in various fields, including pharmaceuticals, agrochemicals, and materials science. The addition of a bromine atom to the 2-methyl position of the thiophene ring modifies its chemical and physical properties, leading to potential applications in different areas.One of the main effects of 4-bromo-2-methylthiophene is its role as a building block for the synthesis of other compounds. The versatility of thiophene derivatives allows for the introduction of various functional groups, which can lead to the formation of diverse chemical compounds. This compound can be used as a starting material for the synthesis of pharmaceutical intermediates, agrochemicals, and other bioactive compounds. Through various synthetic approaches, 4-bromo-2-methylthiophene can be converted into compounds with different pharmacological activities, such as antidepressants, anticonvulsants, and anti-inflammatory agents.Furthermore, the bromine atom attached to the thiophene ring can influence the physicochemical properties of 4-bromo-2-methylthiophene, making it useful in different applications. For example, the bromine atom can enhance the electron-withdrawing capability of the molecule, which can be advantageous for materials science applications. The presence of this electron-withdrawing group can influence the optoelectronic properties, such as absorption and fluorescence, making 4-bromo-2-methylthiophene a potential candidate for use in organic electronic devices, like organic light-emitting diodes (OLEDs) or organic photovoltaics (OPVs).In addition, the bromine atom can also affect the reactivity of 4-bromo-2-methylthiophene, making it useful as a reagent in various chemical reactions. It can act as a nucleophile in substitution reactions or as an electrophile in coupling reactions, enabling the synthesis of complex organic molecules. The reactivity of 4-bromo-2-methylthiophene can be further modified by introducing additional substituents or functional groups to the molecule.In summary, 4-bromo-2-methylthiophene has various effects due to its chemical structure. It can serve as a building block for the synthesis of diverse compounds with potential pharmaceutical or agrochemical applications. Additionally, the presence of the bromine atom can modify the physicochemical properties of the molecule, making it valuable for materials science applications. Finally, its reactivity can be utilized in various chemical reactions, enabling the synthesis of complex organic molecules.