(S)-4-Chloro-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin

98%

Reagent Code: #68677
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CAS Number 137156-22-0

science Other reagents with same CAS 137156-22-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 350.73 g/mol
Formula C₂₀H₁₂ClO₂P
badge Registry Numbers
MDL Number MFCD02093048
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily utilized in asymmetric synthesis, particularly in catalytic processes where it serves as a chiral ligand. It is highly effective in facilitating enantioselective reactions, such as hydrogenation, which are crucial in the production of pharmaceuticals and fine chemicals. Its unique structure allows for precise control over the stereochemistry of the reaction products, ensuring high enantiomeric purity. This makes it invaluable in the synthesis of complex molecules where specific stereochemistry is required for biological activity or desired properties. Additionally, it is employed in the development of advanced materials and in research focused on exploring new catalytic systems.

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Test Parameter Specification
Appearance Colorless to White to Cream to Light Yellow Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿11,862.00
inventory 250mg
10-20 days ฿4,572.00
inventory 5g
10-20 days ฿40,320.00

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(S)-4-Chloro-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin
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This chemical is primarily utilized in asymmetric synthesis, particularly in catalytic processes where it serves as a chiral ligand. It is highly effective in facilitating enantioselective reactions, such as hydrogenation, which are crucial in the production of pharmaceuticals and fine chemicals. Its unique structure allows for precise control over the stereochemistry of the reaction products, ensuring high enantiomeric purity. This makes it invaluable in the synthesis of complex molecules where specific

This chemical is primarily utilized in asymmetric synthesis, particularly in catalytic processes where it serves as a chiral ligand. It is highly effective in facilitating enantioselective reactions, such as hydrogenation, which are crucial in the production of pharmaceuticals and fine chemicals. Its unique structure allows for precise control over the stereochemistry of the reaction products, ensuring high enantiomeric purity. This makes it invaluable in the synthesis of complex molecules where specific stereochemistry is required for biological activity or desired properties. Additionally, it is employed in the development of advanced materials and in research focused on exploring new catalytic systems.

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