(S)-2-([2,2'-Bipyridin]-6-yl)-4-benzyl-4,5-dihydrooxazole

97% 99%ee

Reagent Code: #236920
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CAS Number 2757082-45-2

science Other reagents with same CAS 2757082-45-2

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inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective C–H activation and cross-coupling reactions. Its oxazoline-bipyridine framework coordinates well with transition metals like palladium, copper, and nickel, enhancing stereocontrol in the formation of carbon–carbon and carbon–heteroatom bonds. Commonly applied in the synthesis of pharmaceutical intermediates and fine chemicals where high enantiomeric purity is required. Also employed in the development of new catalytic methodologies due to its robustness and tunable steric and electronic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,250.00
inventory 250mg
10-20 days ฿6,920.00
inventory 1g
10-20 days ฿24,010.00

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(S)-2-([2,2'-Bipyridin]-6-yl)-4-benzyl-4,5-dihydrooxazole
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Used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective C–H activation and cross-coupling reactions. Its oxazoline-bipyridine framework coordinates well with transition metals like palladium, copper, and nickel, enhancing stereocontrol in the formation of carbon–carbon and carbon–heteroatom bonds. Commonly applied in the synthesis of pharmaceutical intermediates and fine chemicals where high enantiomeric purity is required. Also employed in the development of new catalytic method
Used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective C–H activation and cross-coupling reactions. Its oxazoline-bipyridine framework coordinates well with transition metals like palladium, copper, and nickel, enhancing stereocontrol in the formation of carbon–carbon and carbon–heteroatom bonds. Commonly applied in the synthesis of pharmaceutical intermediates and fine chemicals where high enantiomeric purity is required. Also employed in the development of new catalytic methodologies due to its robustness and tunable steric and electronic properties.
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