(3AS,3'aS,7aS,7'aS)-2,2'-[[(1R,3R)-1,3-Dimethyl-1,3-propanediyl]bis(oxy)]bis[octahydro-1,3-diphenyl-1H-1,3,2-benzodiazaphosphole]

98%

Reagent Code: #138272
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CAS Number 1384535-76-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 692.81 g/mol
Formula C₄₁H₅₀N₄O₂P₂
badge Registry Numbers
MDL Number MFCD32173534
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transition metal-catalyzed reactions. It plays a key role in promoting high stereoselectivity in carbon-carbon bond-forming reactions such as hydrogenation, allylic alkylation, and cross-coupling processes. Its rigid, bidentate structure enhances metal-ligand coordination, improving catalytic efficiency and enantiomeric excess in the synthesis of pharmaceuticals and fine chemicals. Commonly employed with palladium, rhodium, or ruthenium complexes, it enables the production of single-enantiomer compounds important in drug development and agrochemicals.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,670.00
inventory 250mg
10-20 days ฿11,630.00
inventory 1g
10-20 days ฿32,310.00
(3AS,3'aS,7aS,7'aS)-2,2'-[[(1R,3R)-1,3-Dimethyl-1,3-propanediyl]bis(oxy)]bis[octahydro-1,3-diphenyl-1H-1,3,2-benzodiazaphosphole]
Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transition metal-catalyzed reactions. It plays a key role in promoting high stereoselectivity in carbon-carbon bond-forming reactions such as hydrogenation, allylic alkylation, and cross-coupling processes. Its rigid, bidentate structure enhances metal-ligand coordination, improving catalytic efficiency and enantiomeric excess in the synthesis of pharmaceuticals and fine chemicals. Commonly employed with palladium, rhodium, or ruthenium complexes, it enables the production of single-enantiomer compounds important in drug development and agrochemicals.
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