Boronic acid, specifically the compound known as 3-[(1,4,7,10-tetraazacyclododec-1-ylacetyl)amino]phenyl]-, monohydrobromide, is a complex organic molecule characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a phenyl ring substituted with an amino group that is further linked to a tetraazacyclododecane moiety, providing a unique structural framework that enhances its potential for coordination chemistry and biological applications. The monohydrobromide form indicates the presence of a bromide ion associated with the molecule, which can influence its solubility and reactivity. Boronic acids are often utilized in organic synthesis, particularly in Suzuki coupling reactions, and may exhibit properties such as pH sensitivity and the ability to form stable complexes with biomolecules. The tetraazacyclododecane structure contributes to the compound's stability and may facilitate interactions with various biological targets, making it of interest in medicinal chemistry and drug development.

Boronic acid,[3-[(1,4,7,10-tetraazacyclododec-1-ylacetyl)amino]phenyl]-,monohydrobromide

800383-20-4: Boronic acid, specifically the compound known as 3-[(1,4,7,10-tetraazacyclododec-1-ylacetyl)amino]phenyl]-, monohydrobromide, is a complex organic molecule characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a phenyl ring substituted with an amino group that is further linked to a tetraazacyclododecane moiety, providing a unique structural framework that enhances its potential for coordination chemistry and biological applications. The monohydrobromide form indicates the presence of a bromide ion associated with the molecule, which can influence its solubility and reactivity. Boronic acids are often utilized in organic synthesis, particularly in Suzuki coupling reactions, and may exhibit properties such as pH sensitivity and the ability to form stable complexes with biomolecules. The tetraazacyclododecane structure contributes to the compound's stability and may facilitate interactions with various biological targets, making it of interest in medicinal chemistry and drug development.

CAS 800383-20-4

Boronic acid,[3-[(1,4,7,10-tetraazacyclododec-1-ylacetyl)amino]phenyl]-,monohydrobromide

Boronic acid,[3-[(1,4,7,10-tetraazacyclododec-1-ylacetyl)amino]phenyl]-,monohydrobromide

Ref: IN-DAN-PC-0UG441