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

98.0%

Reagent Code: #68613
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CAS Number 71042-55-2

science Other reagents with same CAS 71042-55-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 462.51 g/mol
Formula C₃₁H₂₈P₂
badge Registry Numbers
MDL Number MFCD00085365
thermostat Physical Properties
Melting Point 120-125 °C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in transition metal-catalyzed reactions. Its unique bicyclic structure and chiral centers make it highly effective in inducing enantioselectivity in various organic transformations. It is commonly employed in hydrogenation reactions, where it helps produce chiral compounds with high optical purity. Additionally, it finds application in cross-coupling reactions, such as the Suzuki-Miyaura and Heck reactions, to synthesize complex molecules with specific stereochemistry. Its role in catalysis is crucial for the production of pharmaceuticals, agrochemicals, and fine chemicals, where precise control over stereochemistry is essential.

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Test Parameter Specification
Appearance White to almost white crystalline powder
Purity 98-100
Specific rotation [α]20/D (c=1, CHCl3) -51 to -45
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,941.00
inventory 250mg
10-20 days ฿11,952.00
inventory 1g
10-20 days ฿24,912.00

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(2R,3R)-(-)-2,3-Bis(diphenylphosphino)bicyclo[2.2.1]hept-5-ene
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This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in transition metal-catalyzed reactions. Its unique bicyclic structure and chiral centers make it highly effective in inducing enantioselectivity in various organic transformations. It is commonly employed in hydrogenation reactions, where it helps produce chiral compounds with high optical purity. Additionally, it finds application in cross-coupling reactions, such as the Suzuki-Miyaura and Heck reactions, to synthe

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in transition metal-catalyzed reactions. Its unique bicyclic structure and chiral centers make it highly effective in inducing enantioselectivity in various organic transformations. It is commonly employed in hydrogenation reactions, where it helps produce chiral compounds with high optical purity. Additionally, it finds application in cross-coupling reactions, such as the Suzuki-Miyaura and Heck reactions, to synthesize complex molecules with specific stereochemistry. Its role in catalysis is crucial for the production of pharmaceuticals, agrochemicals, and fine chemicals, where precise control over stereochemistry is essential.

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