Phosphinic acid, specifically the compound with the name "[(2S)-3-[[(1S)-1-(3,4-dichlorophenyl)ethyl]amino]-2-hydroxypropyl](phenylmethyl)-," is a phosphinic acid derivative characterized by its complex structure that includes a phosphinic acid functional group, an amino group, and a hydroxypropyl moiety. This compound features a chiral center, contributing to its stereochemistry, which can influence its biological activity and interactions. The presence of the 3,4-dichlorophenyl group suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. Phosphinic acids are known for their ability to act as inhibitors of certain enzymes, making them valuable in various biochemical applications. The compound's solubility, stability, and reactivity can vary based on its specific substituents and the overall molecular structure. As with many phosphinic acid derivatives, it may exhibit unique properties that could be exploited in agrochemicals or therapeutic agents. Safety and handling precautions should be observed due to the potential toxicity associated with chlorinated aromatic compounds.

Phosphinic acid,[(2S)-3-[[(1S)-1-(3,4-dichlorophenyl)ethyl]amino]-2-hydroxypropyl](phenylmethyl)-

150175-54-5: Phosphinic acid, specifically the compound with the name "[(2S)-3-[[(1S)-1-(3,4-dichlorophenyl)ethyl]amino]-2-hydroxypropyl](phenylmethyl)-," is a phosphinic acid derivative characterized by its complex structure that includes a phosphinic acid functional group, an amino group, and a hydroxypropyl moiety. This compound features a chiral center, contributing to its stereochemistry, which can influence its biological activity and interactions. The presence of the 3,4-dichlorophenyl group suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. Phosphinic acids are known for their ability to act as inhibitors of certain enzymes, making them valuable in various biochemical applications. The compound's solubility, stability, and reactivity can vary based on its specific substituents and the overall molecular structure. As with many phosphinic acid derivatives, it may exhibit unique properties that could be exploited in agrochemicals or therapeutic agents. Safety and handling precautions should be observed due to the potential toxicity associated with chlorinated aromatic compounds.

CGP 55845: potent, selective GABAB blocker, IC50=5 nM, hinders agonist binding, reduces GABA/glutamate release.

CAS 150175-54-5

Phosphinic acid,[(2S)-3-[[(1S)-1-(3,4-dichlorophenyl)ethyl]amino]-2-hydroxypropyl](phenylmethyl)-

CGP 55845

Ref: TM-T70531