5-(11bS)-Dinaphtho[2, 1-d: 1', 2'-f][1, 3, 2]dioxaphosphepin-4-yl-10, 11-dihydro-5H-dibenz[b, f]azepine

98%

Reagent Code: #236510
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CAS Number 1361055-01-7

science Other reagents with same CAS 1361055-01-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 509.53 g/mol
Formula C₃₄H₂₄NO₂P
thermostat Physical Properties
Boiling Point 699.4±65.0 °C(Predicted)
inventory_2 Storage & Handling
Storage Room temperature, dry, light-proof

description Product Description

Used as a ligand in palladium-catalyzed cross-coupling reactions, particularly in Suzuki-Miyaura and Buchwald-Hartwig aminations. Its rigid, chiral structure enhances enantioselectivity and catalytic efficiency in asymmetric synthesis. Commonly applied in pharmaceutical manufacturing for constructing carbon-heteroatom and carbon-carbon bonds under mild conditions. Exhibits high thermal stability and electron-donating properties, making it suitable for challenging transformations involving sterically hindered substrates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,100.00
inventory 250mg
10-20 days ฿7,600.00
inventory 1g
10-20 days ฿18,400.00

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5-(11bS)-Dinaphtho[2, 1-d: 1', 2'-f][1, 3, 2]dioxaphosphepin-4-yl-10, 11-dihydro-5H-dibenz[b, f]azepine
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Used as a ligand in palladium-catalyzed cross-coupling reactions, particularly in Suzuki-Miyaura and Buchwald-Hartwig aminations. Its rigid, chiral structure enhances enantioselectivity and catalytic efficiency in asymmetric synthesis. Commonly applied in pharmaceutical manufacturing for constructing carbon-heteroatom and carbon-carbon bonds under mild conditions. Exhibits high thermal stability and electron-donating properties, making it suitable for challenging transformations involving sterically hind

Used as a ligand in palladium-catalyzed cross-coupling reactions, particularly in Suzuki-Miyaura and Buchwald-Hartwig aminations. Its rigid, chiral structure enhances enantioselectivity and catalytic efficiency in asymmetric synthesis. Commonly applied in pharmaceutical manufacturing for constructing carbon-heteroatom and carbon-carbon bonds under mild conditions. Exhibits high thermal stability and electron-donating properties, making it suitable for challenging transformations involving sterically hindered substrates.

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