()-2,3-O-Isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)

99%

Reagent Code: #68610
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Alias (2S,3S)-(+)-1,4-bis(diphenylphosphino)-2,3-O-isopropylidene-2,3-butanediol
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CAS Number 37002-48-5

science Other reagents with same CAS 37002-48-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 498.53 g/mol
Formula C₃₁H₃₂O₂P₂
badge Registry Numbers
MDL Number MFCD00009760
thermostat Physical Properties
Melting Point 86-88 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C, dry, sealed

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in transition metal-catalyzed reactions. Its structure, featuring diphenylphosphino groups, makes it highly effective in coordinating with metals like rhodium, iridium, and palladium, enabling the formation of enantioselective catalysts. These catalysts are widely employed in the production of pharmaceuticals and fine chemicals, where achieving high enantiomeric purity is critical. Additionally, its isopropylidene-protected dihydroxy moiety enhances stability and reactivity, making it suitable for use in complex organic transformations such as hydrogenation, hydroformylation, and cross-coupling reactions. Its application is especially valuable in the synthesis of chiral intermediates for drugs and bioactive molecules.

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Test Parameter Specification
Purity 98.5-100
Specific Rotation [α]20/D (CHCl3) 25-27
Appearance White to light yellow powder
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,560.00
inventory 1g
10-20 days ฿9,550.00

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()-2,3-O-Isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)
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This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in transition metal-catalyzed reactions. Its structure, featuring diphenylphosphino groups, makes it highly effective in coordinating with metals like rhodium, iridium, and palladium, enabling the formation of enantioselective catalysts. These catalysts are widely employed in the production of pharmaceuticals and fine chemicals, where achieving high enantiomeric purity is critical. Additionally, its isopropyliden

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in transition metal-catalyzed reactions. Its structure, featuring diphenylphosphino groups, makes it highly effective in coordinating with metals like rhodium, iridium, and palladium, enabling the formation of enantioselective catalysts. These catalysts are widely employed in the production of pharmaceuticals and fine chemicals, where achieving high enantiomeric purity is critical. Additionally, its isopropylidene-protected dihydroxy moiety enhances stability and reactivity, making it suitable for use in complex organic transformations such as hydrogenation, hydroformylation, and cross-coupling reactions. Its application is especially valuable in the synthesis of chiral intermediates for drugs and bioactive molecules.

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