(11bS)-2,6-Bis(3,5-dimethylphenyl)-4-hydroxy-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin

98%

Reagent Code: #70503
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CAS Number 1170736-59-0

science Other reagents with same CAS 1170736-59-0

blur_circular Chemical Specifications

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Weight 556.6 g/mol
Formula C₃₆H₂₉O₄P
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin core, makes it effective in promoting enantioselective transformations, which are crucial for producing optically active compounds in pharmaceuticals and fine chemicals. Additionally, its sterically hindered and electron-rich aromatic groups enhance its ability to stabilize transition states, improving reaction efficiency and selectivity. It is often employed in metal-catalyzed processes, such as hydrogenation or cross-coupling reactions, where high enantiomeric purity is required. Its application extends to the development of novel therapeutic agents and advanced materials with specific chiral properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,511.00
inventory 250mg
10-20 days ฿6,201.00
inventory 1g
10-20 days ฿20,250.00

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(11bS)-2,6-Bis(3,5-dimethylphenyl)-4-hydroxy-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin
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This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin core, makes it effective in promoting enantioselective transformations, which are crucial for producing optically active compounds in pharmaceuticals and fine chemicals. Additionally, its sterically hindered and electron-rich aromatic groups enhance its ability to stabilize transition state
This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin core, makes it effective in promoting enantioselective transformations, which are crucial for producing optically active compounds in pharmaceuticals and fine chemicals. Additionally, its sterically hindered and electron-rich aromatic groups enhance its ability to stabilize transition states, improving reaction efficiency and selectivity. It is often employed in metal-catalyzed processes, such as hydrogenation or cross-coupling reactions, where high enantiomeric purity is required. Its application extends to the development of novel therapeutic agents and advanced materials with specific chiral properties.
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