(S)-4-((R)-sec-Butyl)-2-(pyridin-2-yl)-4,5-dihydrooxazole

97%

Reagent Code: #68249
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CAS Number 2634687-84-4

science Other reagents with same CAS 2634687-84-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.27 g/mol
Formula C₁₂H₁₆N₂O
inventory_2 Storage & Handling
Storage Room temperature, dark, inert gas

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It facilitates the formation of chiral centers in organic molecules, making it valuable in the production of pharmaceuticals and fine chemicals. Its structure allows it to coordinate with metal catalysts, enhancing their activity and selectivity in reactions such as hydrogenation, cyclopropanation, and cross-coupling. Additionally, it is employed in the development of advanced materials and as a building block in the synthesis of complex organic compounds. Its application in asymmetric catalysis contributes to the efficient and sustainable production of enantiopure substances.

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inventory 50mg
10-20 days ฿3,294.00

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(S)-4-((R)-sec-Butyl)-2-(pyridin-2-yl)-4,5-dihydrooxazole
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This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It facilitates the formation of chiral centers in organic molecules, making it valuable in the production of pharmaceuticals and fine chemicals. Its structure allows it to coordinate with metal catalysts, enhancing their activity and selectivity in reactions such as hydrogenation, cyclopropanation, and cross-coupling. Additionally, it is employed in the deve

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It facilitates the formation of chiral centers in organic molecules, making it valuable in the production of pharmaceuticals and fine chemicals. Its structure allows it to coordinate with metal catalysts, enhancing their activity and selectivity in reactions such as hydrogenation, cyclopropanation, and cross-coupling. Additionally, it is employed in the development of advanced materials and as a building block in the synthesis of complex organic compounds. Its application in asymmetric catalysis contributes to the efficient and sustainable production of enantiopure substances.

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