2,2'-Methylenebis[(4S)-4-phenyl-2-oxazoline]

95%

Reagent Code: #205113
label
Alias 2,2'-methylenebis[(4,s)-4-phenyl-2-oxazoline]
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CAS Number 132098-59-0

science Other reagents with same CAS 132098-59-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 306.36 g/mol
Formula C₁₉H₁₈N₂O₂
badge Registry Numbers
MDL Number MFCD00192295
thermostat Physical Properties
Boiling Point 131-134 °C0.01 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.28 g/mL at 25 °C(lit.)
Storage 2~8°C

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid oxazoline framework enhances stereocontrol in reactions such as cyclopropanations, Diels-Alder, and aldol reactions. Commonly coordinates with metals like copper or palladium to form efficient catalytic systems for producing optically active compounds in pharmaceutical and fine chemical synthesis. Also employed in the development of chiral stationary phases for HPLC due to its ability to differentiate enantiomers.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿1,210.00
100mg
10-20 days ฿1,800.00
250mg
10-20 days ฿4,050.00
1g
10-20 days ฿10,800.00
2,2'-Methylenebis[(4S)-4-phenyl-2-oxazoline]
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid oxazoline framework enhances stereocontrol in reactions such as cyclopropanations, Diels-Alder, and aldol reactions. Commonly coordinates with metals like copper or palladium to form efficient catalytic systems for producing optically active compounds in pharmaceutical and fine chemical synthesis. Also employed in the development of chiral stationary phases for HPLC due to its ability to d

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid oxazoline framework enhances stereocontrol in reactions such as cyclopropanations, Diels-Alder, and aldol reactions. Commonly coordinates with metals like copper or palladium to form efficient catalytic systems for producing optically active compounds in pharmaceutical and fine chemical synthesis. Also employed in the development of chiral stationary phases for HPLC due to its ability to differentiate enantiomers.

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