(1S,2S)-(2-Amino-1-phenylpropyl)diphenylphosphine


Chemical Name: (1S,2S)-(2-Amino-1-phenylpropyl)diphenylphosphine
CAS Number: 341968-71-6
Product Number: AG003BIS(AGN-PC-0WAFUM)
Synonyms:
MDL No:
Molecular Formula: C21H22NP
Molecular Weight: 319.3798

Identification/Properties


Properties
MP:
100-107℃
Storage:
Inert atmosphere;2-8℃;
Form:
Solid

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



(1S,2S)-1-(Diphenylphosphino)-1-phenylpropan-2-amine, commonly known as $name$, is a versatile compound that finds extensive use in chemical synthesis processes. This chiral amine derivative plays a crucial role in the preparation of various pharmaceuticals, agrochemicals, and advanced materials. Its unique stereochemistry and functional groups make it a valuable building block for the creation of complex organic molecules.In chemical synthesis, $name$ is commonly employed as a chiral ligand in asymmetric catalysis. Its phosphine group can effectively coordinate with transition metal catalysts, facilitating asymmetric transformations with high enantioselectivity. This enables the selective production of enantiopure compounds, which is crucial in the pharmaceutical industry where the activity and safety of a drug often depend on its chirality.Additionally, (1S,2S)-1-(Diphenylphosphino)-1-phenylpropan-2-amine is utilized in the synthesis of ligands for homogeneous catalysis, where it can control the stereochemistry of chemical reactions. It can also be used in asymmetric hydrogenation processes, cross-coupling reactions, and other transformations that require enantioselective control.Overall, the application of $name$ in chemical synthesis showcases its significance as a valuable tool for constructing complex molecules with high stereochemical precision and efficiency.