Bis((S)-4-benzyl-4,5-dihydrooxazol-2-yl)methane

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Reagent Code: #55877
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CAS Number 132098-58-9

science Other reagents with same CAS 132098-58-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 334.4116 g/mol
Formula C₂₁H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD00198096
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, cyclopropanation, and other carbon-carbon bond-forming reactions. Its structure allows it to coordinate effectively with transition metals, enhancing the selectivity and efficiency of the catalytic process. This makes it valuable in the production of pharmaceuticals and fine chemicals, where achieving high enantiomeric purity is essential. Additionally, it is employed in academic research to develop new methodologies in organic synthesis.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,835.00

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Bis((S)-4-benzyl-4,5-dihydrooxazol-2-yl)methane
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This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, cyclopropanation, and other carbon-carbon bond-forming reactions. Its structure allows it to coordinate effectively with transition metals, enhancing the selectivity and efficiency of the catalytic process. This makes it valuable in the production of pharmaceuticals and fine chemicals, where ac

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, cyclopropanation, and other carbon-carbon bond-forming reactions. Its structure allows it to coordinate effectively with transition metals, enhancing the selectivity and efficiency of the catalytic process. This makes it valuable in the production of pharmaceuticals and fine chemicals, where achieving high enantiomeric purity is essential. Additionally, it is employed in academic research to develop new methodologies in organic synthesis.

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