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

98%

Reagent Code: #68680
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CAS Number 1107608-80-9

science Other reagents with same CAS 1107608-80-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 334.38 g/mol
Formula C₁₈H₂₈N₂P₂
badge Registry Numbers
MDL Number MFCD10567042
thermostat Physical Properties
Melting Point 102°C
inventory_2 Storage & Handling
Storage room temperature, in an inert gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as hydrogenation, hydroformylation, and cross-coupling reactions. Its unique steric and electronic properties enhance enantioselectivity, making it valuable in the synthesis of pharmaceuticals and fine chemicals. It is also employed in the development of stereospecific polymers and advanced materials.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to light yellow to yellow to orange to brown to tan powder or crystals
Purity 97.5-100
Specific rotation [α]_D^{20} (c=1, CHCl3) 50.0
Melting Point 100.0-104.0
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿16,890.00
inventory 10mg
10-20 days ฿2,630.00
inventory 50mg
10-20 days ฿3,630.00

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(S,S)-()-2,3-Bis(tert-butylmethylphosphino)quinoxaline
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Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as hydrogenation, hydroformylation, and cross-coupling reactions. Its unique steric and electronic properties enhance enantioselectivity, making it valuable in the synthesis of pharmaceuticals and fine chemicals. It is also employed in the development of stereospecific polymers and advanced materials.

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as hydrogenation, hydroformylation, and cross-coupling reactions. Its unique steric and electronic properties enhance enantioselectivity, making it valuable in the synthesis of pharmaceuticals and fine chemicals. It is also employed in the development of stereospecific polymers and advanced materials.

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