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

98%

Reagent Code: #229420
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CAS Number 1045894-43-6

science Other reagents with same CAS 1045894-43-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.25 g/mol
Formula C₁₂H₁₅NO₂
badge Registry Numbers
MDL Number MFCD29076255
thermostat Physical Properties
Boiling Point 327.8±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.16±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, 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 group allows coordination to metal centers, making it valuable in the development of catalysts for reactions such as enantioselective hydrogenation or carbon-carbon bond formation. Commonly employed in pharmaceutical and fine chemical synthesis to produce single-enantiomer compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,270.00
inventory 250mg
10-20 days ฿22,450.00

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(R)-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 group allows coordination to metal centers, making it valuable in the development of catalysts for reactions such as enantioselective hydrogenation or carbon-carbon bond formation. Commonly employed in pharmaceutical and fine chemical synthesis to produce single-enantiomer compounds.

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 group allows coordination to metal centers, making it valuable in the development of catalysts for reactions such as enantioselective hydrogenation or carbon-carbon bond formation. Commonly employed in pharmaceutical and fine chemical synthesis to produce single-enantiomer compounds.

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