(R,R)-(-)-2,3-Bis(tert-butylmethylphosphino)quinoxaline

98%

Reagent Code: #230306
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CAS Number 866081-62-1

science Other reagents with same CAS 866081-62-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 334.38 g/mol
Formula C₁₈H₂₈N₂P₂
badge Registry Numbers
MDL Number MFCD10565649
inventory_2 Storage & Handling
Storage Room temperature, stored in inert gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in transition-metal-catalyzed reactions. It plays a key role in enantioselective transformations such as hydrogenation, coupling reactions, and carbon-carbon bond formations. Its rigid quinoxaline backbone and bulky tert-butyl groups enhance stereocontrol, leading to high enantiomeric excess in products. Commonly employed with rhodium, ruthenium, or palladium complexes in pharmaceutical synthesis and fine chemical manufacturing where precise chirality is required.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿1,950.00
inventory 50mg
10-20 days ฿3,290.00
inventory 250mg
10-20 days ฿10,660.00
inventory 1g
10-20 days ฿37,200.00

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(R,R)-(-)-2,3-Bis(tert-butylmethylphosphino)quinoxaline
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Used as a chiral ligand in asymmetric catalysis, particularly in transition-metal-catalyzed reactions. It plays a key role in enantioselective transformations such as hydrogenation, coupling reactions, and carbon-carbon bond formations. Its rigid quinoxaline backbone and bulky tert-butyl groups enhance stereocontrol, leading to high enantiomeric excess in products. Commonly employed with rhodium, ruthenium, or palladium complexes in pharmaceutical synthesis and fine chemical manufacturing where precise c

Used as a chiral ligand in asymmetric catalysis, particularly in transition-metal-catalyzed reactions. It plays a key role in enantioselective transformations such as hydrogenation, coupling reactions, and carbon-carbon bond formations. Its rigid quinoxaline backbone and bulky tert-butyl groups enhance stereocontrol, leading to high enantiomeric excess in products. Commonly employed with rhodium, ruthenium, or palladium complexes in pharmaceutical synthesis and fine chemical manufacturing where precise chirality is required.

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