(S)-2-(4-Isopropyl-4,5-dihydrooxazol-2-yl)phenol

95%

Reagent Code: #236619
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CAS Number 131380-91-1

science Other reagents with same CAS 131380-91-1

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Weight 205.25 g/mol
Formula C₁₂H₁₅NO₂
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral ligand or intermediate in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. Its oxazoline core combined with a phenolic hydroxyl group allows coordination to metal centers, making it valuable in the development of catalysts for enantioselective transformations such as hydrogenations, carbon-carbon bond formations, or epoxidations. The compound’s stereochemistry enhances selectivity in pharmaceutical synthesis, where production of a single enantiomer is often required. It may also serve as a building block in the preparation of more complex chiral molecules used in medicinal chemistry and fine chemical manufacturing.

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inventory 100mg
10-20 days ฿4,470.00

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(S)-2-(4-Isopropyl-4,5-dihydrooxazol-2-yl)phenol
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Used as a chiral ligand or intermediate in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. Its oxazoline core combined with a phenolic hydroxyl group allows coordination to metal centers, making it valuable in the development of catalysts for enantioselective transformations such as hydrogenations, carbon-carbon bond formations, or epoxidations. The compound’s stereochemistry enhances selectivity in pharmaceutical synthesis, where production of a single enan

Used as a chiral ligand or intermediate in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. Its oxazoline core combined with a phenolic hydroxyl group allows coordination to metal centers, making it valuable in the development of catalysts for enantioselective transformations such as hydrogenations, carbon-carbon bond formations, or epoxidations. The compound’s stereochemistry enhances selectivity in pharmaceutical synthesis, where production of a single enantiomer is often required. It may also serve as a building block in the preparation of more complex chiral molecules used in medicinal chemistry and fine chemical manufacturing.

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