1,3-Bis((R)-1-(naphthalen-1-yl)ethyl)-1,3,2-diazaphospholidine2-oxide

98%

Reagent Code: #155932
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CAS Number 1449218-81-8

science Other reagents with same CAS 1449218-81-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 414.48 g/mol
Formula C₂₆H₂₇N₂OP
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral organocatalyst in asymmetric synthesis, particularly in enantioselective phosphorylation and C–C bond-forming reactions. Its rigid naphthyl-containing structure enhances stereocontrol, making it valuable in the preparation of optically active pharmaceuticals and fine chemicals. The compound is also employed in coordination chemistry as a ligand for transition metals in catalytic systems, supporting asymmetric hydrogenation and transfer hydrogenation processes. Its phosphorus center and stereogenic sites contribute to high enantioselectivity in various transformations.

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inventory 250mg
10-20 days ฿21,930.00

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1,3-Bis((R)-1-(naphthalen-1-yl)ethyl)-1,3,2-diazaphospholidine2-oxide
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Used as a chiral organocatalyst in asymmetric synthesis, particularly in enantioselective phosphorylation and C–C bond-forming reactions. Its rigid naphthyl-containing structure enhances stereocontrol, making it valuable in the preparation of optically active pharmaceuticals and fine chemicals. The compound is also employed in coordination chemistry as a ligand for transition metals in catalytic systems, supporting asymmetric hydrogenation and transfer hydrogenation processes. Its phosphorus center and s

Used as a chiral organocatalyst in asymmetric synthesis, particularly in enantioselective phosphorylation and C–C bond-forming reactions. Its rigid naphthyl-containing structure enhances stereocontrol, making it valuable in the preparation of optically active pharmaceuticals and fine chemicals. The compound is also employed in coordination chemistry as a ligand for transition metals in catalytic systems, supporting asymmetric hydrogenation and transfer hydrogenation processes. Its phosphorus center and stereogenic sites contribute to high enantioselectivity in various transformations.

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