Boronic acid, specifically the compound known as B-[4-[5-(methylamino)-1,3,4-thiadiazol-2-yl]phenyl]- (CAS number 957034-49-0), is characterized by its boron-containing functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a phenyl ring substituted with a thiadiazole moiety, which contributes to its biological activity and potential applications in medicinal chemistry. The presence of a methylamino group enhances its solubility and reactivity, making it suitable for various chemical reactions, including Suzuki coupling, which is pivotal in organic synthesis. Boronic acids are also recognized for their role in drug development, particularly in targeting specific biological pathways. Additionally, this compound may exhibit unique properties such as fluorescence or specific binding affinities, depending on its structural configuration. Overall, the characteristics of this boronic acid derivative suggest its utility in both synthetic and pharmaceutical chemistry, warranting further investigation into its potential applications.

Boronic acid,B-[4-[5-(methylamino)-1,3,4-thiadiazol-2-yl]phenyl]-

957034-49-0: 4-(5-(Methylamino)-1,3,4-thiadiazol-2-yl)phenylboronic acid

4-[5-(Methylamino)-1,3,4-thiadiazol-2-yl]benzeneboronic acid

4-(5-(Methylamino)-1,3,4-thiadiazol-2-yl)phenylboronic acid

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CAS 957034-49-0: Boronic acid,B-[4-[5-(methylamino)-1,3,4-thiadiazol-2-yl]phenyl]-

4-[5-(Methylamino)-1,3,4-thiadiazol-2-yl]benzeneboronic acid

Ref: 54-OR8581

4-(5-(Methylamino)-1,3,4-thiadiazol-2-yl)phenylboronic acid

Ref: IN-DA006BSM

4-(5-(Methylamino)-1,3,4-thiadiazol-2-yl)phenylboronic acid

Ref: 3D-FM161017