1-Bromomethyl-o-carborane is a chemical compound that belongs to the class of carboranes, which are polyhedral boron-carbon clusters. This particular compound features a bromomethyl group (-CH2Br) attached to the o-carborane structure, which consists of a cage-like arrangement of boron and carbon atoms. The presence of the bromomethyl group introduces reactivity, making it useful in various chemical reactions, including nucleophilic substitutions and coupling reactions. 1-Bromomethyl-o-carborane is characterized by its stability under ambient conditions, although it may undergo reactions typical of alkyl halides. The compound is of interest in materials science and medicinal chemistry due to its unique structural properties and potential applications in drug delivery systems and as a building block for more complex molecules. Its solubility characteristics can vary depending on the solvent, and it is generally handled with care due to the presence of the bromine atom, which can be reactive. Overall, 1-Bromomethyl-o-carborane exemplifies the intriguing chemistry associated with carborane derivatives.

1-Bromomethyl-o-carborane

19496-84-5: 1-Bromomethyl-o-carborane is a chemical compound that belongs to the class of carboranes, which are polyhedral boron-carbon clusters. This particular compound features a bromomethyl group (-CH2Br) attached to the o-carborane structure, which consists of a cage-like arrangement of boron and carbon atoms. The presence of the bromomethyl group introduces reactivity, making it useful in various chemical reactions, including nucleophilic substitutions and coupling reactions. 1-Bromomethyl-o-carborane is characterized by its stability under ambient conditions, although it may undergo reactions typical of alkyl halides. The compound is of interest in materials science and medicinal chemistry due to its unique structural properties and potential applications in drug delivery systems and as a building block for more complex molecules. Its solubility characteristics can vary depending on the solvent, and it is generally handled with care due to the presence of the bromine atom, which can be reactive. Overall, 1-Bromomethyl-o-carborane exemplifies the intriguing chemistry associated with carborane derivatives.

1-Bromomethyl-o-carborane is a boron compound that has been used as a cross-coupling reagent for the conversion of terminal alkynes to acetonitrile. This reagent is prepared by the reaction of lithium diisopropylamide with dicarbonyl compounds, followed by desilylation and alkylation. The hydroxy group can be substituted with triflates or monosubstituted groups. The nature of these substituents will depend on the desired product and reaction conditions. 1-Bromomethyl-o-carborane has been shown to form hyaluronic acid in yields of up to 98%.

CAS 19496-84-5

1-Bromomethyl-o-carborane

1-Bromomethyl-o-carborane

Ref: 3D-FB45712