(R)-2-([2,2'-Bipyridin]-6-yl)-4-isopropyl-4,5-dihydrooxazole

97%

Reagent Code: #231381
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CAS Number 2757082-46-3

science Other reagents with same CAS 2757082-46-3

blur_circular Chemical Specifications

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

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transformations such as carbon–carbon bond-forming reactions. Its structure enables strong coordination to transition metals like copper or nickel, enhancing stereocontrol in reactions including conjugate additions and cyclopropanations. Due to its rigid bipyridine core and stereogenic center, it helps achieve high enantiomeric excess in the synthesis of pharmaceutical intermediates and fine chemicals. Commonly employed in research settings for developing catalytic methods where precise stereochemistry is critical.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿4,940.00
1g
10-20 days ฿24,870.00
250mg
10-20 days ฿7,730.00
(R)-2-([2,2'-Bipyridin]-6-yl)-4-isopropyl-4,5-dihydrooxazole
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transformations such as carbon–carbon bond-forming reactions. Its structure enables strong coordination to transition metals like copper or nickel, enhancing stereocontrol in reactions including conjugate additions and cyclopropanations. Due to its rigid bipyridine core and stereogenic center, it helps achieve high enantiomeric excess in the synthesis of pharmaceutical intermediates and fine chemicals. Commonly employed in res
Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transformations such as carbon–carbon bond-forming reactions. Its structure enables strong coordination to transition metals like copper or nickel, enhancing stereocontrol in reactions including conjugate additions and cyclopropanations. Due to its rigid bipyridine core and stereogenic center, it helps achieve high enantiomeric excess in the synthesis of pharmaceutical intermediates and fine chemicals. Commonly employed in research settings for developing catalytic methods where precise stereochemistry is critical.
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