(2S,3S)-()-2,3-Bis(diphenylphosphino)bicyclo[2.2.1]hept-5-ene

98.0%

Reagent Code: #68621
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CAS Number 71042-54-1

science Other reagents with same CAS 71042-54-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 462.51 g/mol
Formula C₃₁H₂₈P₂
badge Registry Numbers
MDL Number MFCD00085364
thermostat Physical Properties
Melting Point 120 °C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure allows it to facilitate enantioselective transformations, making it valuable in the synthesis of pharmaceuticals and fine chemicals. It is often employed in hydrogenation, hydroformylation, and carbon-carbon bond-forming reactions, where high enantiomeric purity is crucial. Additionally, its bicyclic framework provides stability and steric control, enhancing the efficiency and selectivity of catalytic processes.

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Test Parameter Specification
Purity (GC) 98-100%
Specific Rotation (20°C, CHCl3) 45-51
Infrared Spectrometry Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,800.00
inventory 250mg
10-20 days ฿22,780.00

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(2S,3S)-()-2,3-Bis(diphenylphosphino)bicyclo[2.2.1]hept-5-ene
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This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure allows it to facilitate enantioselective transformations, making it valuable in the synthesis of pharmaceuticals and fine chemicals. It is often employed in hydrogenation, hydroformylation, and carbon-carbon bond-forming reactions, where high enantiomeric purity is crucial. Additionally, its bicyclic framework provides stability and steric control, enhancing

This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure allows it to facilitate enantioselective transformations, making it valuable in the synthesis of pharmaceuticals and fine chemicals. It is often employed in hydrogenation, hydroformylation, and carbon-carbon bond-forming reactions, where high enantiomeric purity is crucial. Additionally, its bicyclic framework provides stability and steric control, enhancing the efficiency and selectivity of catalytic processes.

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