(R)-BoroPhe-(+)-Pinanediol, with the CAS number 186906-12-7, is a chiral boron-containing compound that plays a significant role in organic synthesis and catalysis. This compound features a boron atom bonded to a phenyl group and a pinanediol moiety, which contributes to its stereochemical properties. The presence of the boron atom allows for unique reactivity, particularly in forming boron-oxygen and boron-carbon bonds, making it useful in various synthetic applications, including asymmetric synthesis. The pinanediol component provides steric hindrance and can influence the selectivity of reactions. Additionally, the chirality of the compound can be leveraged in enantioselective processes, which are crucial in the production of pharmaceuticals and agrochemicals. Its solubility characteristics and stability under various conditions further enhance its utility in laboratory settings. Overall, (R)-BoroPhe-(+)-Pinanediol exemplifies the intersection of organoboron chemistry and stereochemistry, showcasing its importance in modern synthetic methodologies.

(R)-BoroPhe-(+)-Pinanediol

186906-12-7: (R)-BoroPhe-(+)-Pinanediol, with the CAS number 186906-12-7, is a chiral boron-containing compound that plays a significant role in organic synthesis and catalysis. This compound features a boron atom bonded to a phenyl group and a pinanediol moiety, which contributes to its stereochemical properties. The presence of the boron atom allows for unique reactivity, particularly in forming boron-oxygen and boron-carbon bonds, making it useful in various synthetic applications, including asymmetric synthesis. The pinanediol component provides steric hindrance and can influence the selectivity of reactions. Additionally, the chirality of the compound can be leveraged in enantioselective processes, which are crucial in the production of pharmaceuticals and agrochemicals. Its solubility characteristics and stability under various conditions further enhance its utility in laboratory settings. Overall, (R)-BoroPhe-(+)-Pinanediol exemplifies the intersection of organoboron chemistry and stereochemistry, showcasing its importance in modern synthetic methodologies.

<p>(R)-Borophenylalanine-(1S,2S,3R,5S)-(+)-2,3-pinanediol ester hydrochloride</p>

CAS 186906-12-7

(R)-BoroPhe-(+)-Pinanediol

(R)-BoroPhe-(+)-Pinanediol

Ref: IN-DA00AQ5A

(R)-Borophenylalanine-(1S,2S,3R,5S)-(+)-2,3-pinanediol ester hydrochloride

Ref: 54-OR310267