
CAS 1132832-75-7
:Methanone, (5-Bromo-2-methylphenyl)[5-(4-fluorophenyl)-2-thienyl]-
Description:
Methanone, (5-Bromo-2-methylphenyl)[5-(4-fluorophenyl)-2-thienyl]- is an organic compound characterized by its complex structure, which includes a methanone functional group and multiple aromatic rings. The presence of bromine and fluorine substituents indicates that this compound may exhibit unique electronic properties and reactivity patterns, making it of interest in various chemical applications, including pharmaceuticals and agrochemicals. The thienyl group contributes to its heterocyclic nature, potentially enhancing its biological activity. Additionally, the compound's molecular structure suggests it may participate in various chemical reactions, such as electrophilic aromatic substitution or nucleophilic attacks, due to the electron-withdrawing effects of the halogen atoms. Its solubility and stability can be influenced by the substituents on the aromatic rings, which may also affect its interaction with biological targets. Overall, this compound exemplifies the complexity and diversity of organic molecules, particularly those with halogenated and heterocyclic components.
Formula:C18H12BrFOS
Synonyms:- (5-Bromo-2-Methylphenyl)-(5-(4-Fluorophenyl)-2-Thienyl)Methanone
- 2-(5-Bromo-2-Methylbenzoyl)-5-(4-Fluorophenyl)Thiophene
- (5-broMo-2-Methylphenyl)(5-(4-fluorophenyl)thiophen-2-yl)Methanone
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Found 5 products.
2-(5-Bromo-2-methylbenzoyl)-5-(4-fluorophenyl)thiophene
CAS:Formula:C18H12BrFOSPurity:97%Color and Shape:SolidMolecular weight:375.25472-(5-Bromo-2-methylbenzoyl)-5-(4-fluorophenyl)thiophene
CAS:2-(5-Bromo-2-methylbenzoyl)-5-(4-fluorophenyl)thiophenePurity:98%Molecular weight:375.25g/mol(5-Bromo-2-methylphenyl)(5-(4-fluorophenyl)thiophen-2-yl)methanone
CAS:Purity:95.0%Molecular weight:375.2600097656252-(5-Bromo-2-methylbenzoyl)-5-(4-fluorophenyl)thiophene
CAS:Controlled Product<p>Applications 2-(5-Bromo-2-methylbenzoyl)-5-(4-fluorophenyl)thiophene is an intermediate in the preparation of Canagliflozin which is a sodium-dependent glucose co-transporter 2 inhibitor used in the treatment of type 2 diabetes.<br>References Nomura, S., et al.: J. Med. Chem., 53, 6355 (2010);<br></p>Formula:C18H12BrFOSColor and Shape:NeatMolecular weight:375.25




