(4S,4'S)-2,2'-(2,3-Dihydro-1H-indene-2,2-diyl)bis(4-benzyl-4,5-dihydrooxazole)

97%

Reagent Code: #69981
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CAS Number 1003886-09-6

science Other reagents with same CAS 1003886-09-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 436.54 g/mol
Formula C₂₉H₂₈N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in facilitating enantioselective reactions, particularly in the formation of carbon-carbon or carbon-heteroatom bonds, which are crucial in the production of pharmaceuticals and fine chemicals. Its application is prominent in organic transformations such as hydrogenation, cyclopropanation, and other stereospecific reactions, where high enantiomeric purity is required. The compound’s rigid structure and chiral environment make it effective in controlling the stereochemistry of the reaction products, ensuring the desired enantiomer is obtained with high selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,691.00

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(4S,4'S)-2,2'-(2,3-Dihydro-1H-indene-2,2-diyl)bis(4-benzyl-4,5-dihydrooxazole)
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This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in facilitating enantioselective reactions, particularly in the formation of carbon-carbon or carbon-heteroatom bonds, which are crucial in the production of pharmaceuticals and fine chemicals. Its application is prominent in organic transformations such as hydrogenation, cyclopropanation, and other stereospecific reactions, where high enantiomeric purity is required. The compound’s rig

This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in facilitating enantioselective reactions, particularly in the formation of carbon-carbon or carbon-heteroatom bonds, which are crucial in the production of pharmaceuticals and fine chemicals. Its application is prominent in organic transformations such as hydrogenation, cyclopropanation, and other stereospecific reactions, where high enantiomeric purity is required. The compound’s rigid structure and chiral environment make it effective in controlling the stereochemistry of the reaction products, ensuring the desired enantiomer is obtained with high selectivity.

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