(R)-3-(tert-Butyl)-4-(3,5-diisopropyl-2,6-dimethoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole

97%

Reagent Code: #55104
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CAS Number 2351219-90-2

science Other reagents with same CAS 2351219-90-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 414.5100 g/mol
Formula C₂₅H₃₅O₃P
badge Registry Numbers
MDL Number MFCD32641161
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized in the field of asymmetric synthesis and catalysis, particularly in the development of chiral ligands. Its unique structure makes it highly effective in facilitating enantioselective reactions, which are crucial for producing optically active compounds in pharmaceuticals and fine chemicals. The compound is often employed in transition metal-catalyzed processes, such as hydrogenation, where it enhances the selectivity and efficiency of the reaction. Additionally, it finds application in the synthesis of complex organic molecules, where its stereochemical properties help control the spatial arrangement of atoms, leading to the desired chiral products. Its use is particularly prominent in the production of active pharmaceutical ingredients (APIs) that require high enantiomeric purity.

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Test Parameter Specification
Appearance White to off-white solid
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,770.00
inventory 500mg
10-20 days ฿48,600.00

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(R)-3-(tert-Butyl)-4-(3,5-diisopropyl-2,6-dimethoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole
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This chemical is primarily utilized in the field of asymmetric synthesis and catalysis, particularly in the development of chiral ligands. Its unique structure makes it highly effective in facilitating enantioselective reactions, which are crucial for producing optically active compounds in pharmaceuticals and fine chemicals. The compound is often employed in transition metal-catalyzed processes, such as hydrogenation, where it enhances the selectivity and efficiency of the reaction. Additionally, it fin

This chemical is primarily utilized in the field of asymmetric synthesis and catalysis, particularly in the development of chiral ligands. Its unique structure makes it highly effective in facilitating enantioselective reactions, which are crucial for producing optically active compounds in pharmaceuticals and fine chemicals. The compound is often employed in transition metal-catalyzed processes, such as hydrogenation, where it enhances the selectivity and efficiency of the reaction. Additionally, it finds application in the synthesis of complex organic molecules, where its stereochemical properties help control the spatial arrangement of atoms, leading to the desired chiral products. Its use is particularly prominent in the production of active pharmaceutical ingredients (APIs) that require high enantiomeric purity.

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