(-)-6,6'-[(1S,3S)-1,3-Dimethyl-1,3-propanediyl]bis(oxy)bis[4,8-bis(t-butyl)-2,10-dimethoxy-bibenzo[d,f][1,3,2]dioxaphosphepin]

98%

Reagent Code: #68570
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CAS Number 852042-07-0

science Other reagents with same CAS 852042-07-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 876.99 g/mol
Formula C₄₉H₆₆O₁₀P₂
badge Registry Numbers
MDL Number MFCD06798297
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure allows it to induce high enantioselectivity in various organic transformations, such as hydrogenation, carbon-carbon bond formation, and oxidation reactions. It is particularly valuable in the synthesis of pharmaceuticals and fine chemicals, where controlling the stereochemistry of the product is crucial. The compound’s sterically hindered and electron-rich environment enhances its ability to stabilize metal complexes and direct the reaction pathway toward the desired enantiomer. Its application is significant in producing chiral intermediates for drugs, agrochemicals, and other high-value compounds.

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Test Parameter Specification
Appearance White to off-white Solid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿6,228.00
inventory 250mg
10-20 days ฿15,858.00
inventory 1g
10-20 days ฿41,220.00

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(-)-6,6'-[(1S,3S)-1,3-Dimethyl-1,3-propanediyl]bis(oxy)bis[4,8-bis(t-butyl)-2,10-dimethoxy-bibenzo[d,f][1,3,2]dioxaphosphepin]
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This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure allows it to induce high enantioselectivity in various organic transformations, such as hydrogenation, carbon-carbon bond formation, and oxidation reactions. It is particularly valuable in the synthesis of pharmaceuticals and fine chemicals, where controlling the stereochemistry of the product is crucial. The compound’s sterically hindered and electron-ric

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure allows it to induce high enantioselectivity in various organic transformations, such as hydrogenation, carbon-carbon bond formation, and oxidation reactions. It is particularly valuable in the synthesis of pharmaceuticals and fine chemicals, where controlling the stereochemistry of the product is crucial. The compound’s sterically hindered and electron-rich environment enhances its ability to stabilize metal complexes and direct the reaction pathway toward the desired enantiomer. Its application is significant in producing chiral intermediates for drugs, agrochemicals, and other high-value compounds.

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