Phospholane, 1,1'-(1,2-phenylene)bis[2,5-diethyl-, (2R,2'R,5R,5'R)-


Chemical Name: Phospholane, 1,1'-(1,2-phenylene)bis[2,5-diethyl-, (2R,2'R,5R,5'R)-
CAS Number: 136705-64-1
Product Number: AG00129H(AGN-PC-0PL1PM)
Synonyms:
MDL No:
Molecular Formula: C22H36P2
Molecular Weight: 362.4688

Identification/Properties


Properties
BP:
bp0.045 138-145°
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Stability:
Air Sensitive
Refractive Index:
n 20/D 1.6

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



1,2-Bis((2R,5R)-2,5-diethylphospholan-1-yl)benzene, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role as a chiral ligand in various catalytic processes, particularly in asymmetric synthesis. By acting as a ligand in metal-catalyzed reactions, $name$ facilitates the selective formation of chiral molecules, enabling the production of enantiomerically pure compounds.In organic chemistry, the application of $name$ is significant in mediating a range of transformations, such as asymmetric hydrogenation, cross-coupling reactions, and cycloadditions. Its unique structure, featuring chiral phospholane groups, imparts high stereocontrol in these reactions, leading to the synthesis of complex molecules with exceptional enantiomeric purity.Moreover, the use of 1,2-Bis((2R,5R)-2,5-diethylphospholan-1-yl)benzene is prevalent in pharmaceutical research and fine chemical synthesis, where precise control over the stereochemistry of molecules is crucial for their biological activity or material properties. Overall, this compound serves as a valuable tool in the hands of chemists, enabling the efficient and selective construction of chiral compounds with synthetic versatility and high purity.