2,6-Bis((R)-4-methyl-4,5-dihydrooxazol-2-yl)pyridine

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Reagent Code: #41042
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CAS Number 256377-24-9

science Other reagents with same CAS 256377-24-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.2771 g/mol
Formula C₁₃H₁₅N₃O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in metal-catalyzed reactions. Its structure, featuring two oxazoline rings, allows it to effectively coordinate with transition metals like palladium, copper, and nickel, enabling the synthesis of enantiomerically pure compounds. It is widely applied in organic synthesis for the production of pharmaceuticals, agrochemicals, and fine chemicals, where high enantioselectivity is crucial. Additionally, its stability and tunable steric and electronic properties make it a valuable tool in developing efficient catalytic systems for C-C bond formation and other transformation processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿570.00
inventory 1g
10-20 days ฿3,840.00
inventory 5g
10-20 days ฿15,850.00
inventory 250mg
10-20 days ฿1,250.00

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2,6-Bis((R)-4-methyl-4,5-dihydrooxazol-2-yl)pyridine
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This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in metal-catalyzed reactions. Its structure, featuring two oxazoline rings, allows it to effectively coordinate with transition metals like palladium, copper, and nickel, enabling the synthesis of enantiomerically pure compounds. It is widely applied in organic synthesis for the production of pharmaceuticals, agrochemicals, and fine chemicals, where high enantioselectivity is crucial. Additionally, its stability

This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in metal-catalyzed reactions. Its structure, featuring two oxazoline rings, allows it to effectively coordinate with transition metals like palladium, copper, and nickel, enabling the synthesis of enantiomerically pure compounds. It is widely applied in organic synthesis for the production of pharmaceuticals, agrochemicals, and fine chemicals, where high enantioselectivity is crucial. Additionally, its stability and tunable steric and electronic properties make it a valuable tool in developing efficient catalytic systems for C-C bond formation and other transformation processes.

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