(2S,2'S)-()-2,2'-Bipyrrolidine

99%

Reagent Code: #235923
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CAS Number 124779-66-4

science Other reagents with same CAS 124779-66-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 140.23 g/mol
Formula C₈H₁₆N
badge Registry Numbers
MDL Number MFCD12911901
thermostat Physical Properties
Boiling Point 79 - 81 °C at 3 mmHg (lit.)
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral ligand in asymmetric catalysis, enabling the synthesis of enantiomerically enriched compounds in pharmaceuticals and fine chemicals. Its rigid, bidentate structure enhances stereocontrol in transition-metal-catalyzed reactions such as aldol, Mannich, and Michael additions. Also employed in organocatalysis for promoting carbon–carbon bond-forming reactions with high enantioselectivity. Soluble in common organic solvents, it facilitates homogeneous reaction conditions and is often paired with copper or nickel complexes for improved catalytic efficiency.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿19,090.00

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(2S,2'S)-()-2,2'-Bipyrrolidine
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Used as a chiral ligand in asymmetric catalysis, enabling the synthesis of enantiomerically enriched compounds in pharmaceuticals and fine chemicals. Its rigid, bidentate structure enhances stereocontrol in transition-metal-catalyzed reactions such as aldol, Mannich, and Michael additions. Also employed in organocatalysis for promoting carbon–carbon bond-forming reactions with high enantioselectivity. Soluble in common organic solvents, it facilitates homogeneous reaction conditions and is often paired w

Used as a chiral ligand in asymmetric catalysis, enabling the synthesis of enantiomerically enriched compounds in pharmaceuticals and fine chemicals. Its rigid, bidentate structure enhances stereocontrol in transition-metal-catalyzed reactions such as aldol, Mannich, and Michael additions. Also employed in organocatalysis for promoting carbon–carbon bond-forming reactions with high enantioselectivity. Soluble in common organic solvents, it facilitates homogeneous reaction conditions and is often paired with copper or nickel complexes for improved catalytic efficiency.

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