(3aR,3'aR,8aS,8'aS)-2,2'-(1-Methylethylidene)bis[3a,8a-dihydro-8H-indeno[1,2-d]oxazole]

≥97%

Reagent Code: #57551
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CAS Number 189623-45-8

science Other reagents with same CAS 189623-45-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 358.4 g/mol
Formula C₂₃H₂₂N₂O₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in the field of organic synthesis, where it serves as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a rigid framework and stereogenic centers, makes it highly effective in controlling the stereochemistry of reactions, particularly in the synthesis of enantiomerically pure compounds. It is often employed in pharmaceutical research and development to produce chiral intermediates or active pharmaceutical ingredients (APIs) with high enantioselectivity. Additionally, it finds application in materials science for the development of advanced chiral materials, such as liquid crystals or polymers with specific optical properties. Its role in enhancing the efficiency and selectivity of chemical processes makes it a valuable tool in both academic and industrial settings.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,241.00

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(3aR,3'aR,8aS,8'aS)-2,2'-(1-Methylethylidene)bis[3a,8a-dihydro-8H-indeno[1,2-d]oxazole]
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This chemical is primarily utilized in the field of organic synthesis, where it serves as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a rigid framework and stereogenic centers, makes it highly effective in controlling the stereochemistry of reactions, particularly in the synthesis of enantiomerically pure compounds. It is often employed in pharmaceutical research and development to produce chiral intermediates or active pharmaceutical ingredients (APIs) with high

This chemical is primarily utilized in the field of organic synthesis, where it serves as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a rigid framework and stereogenic centers, makes it highly effective in controlling the stereochemistry of reactions, particularly in the synthesis of enantiomerically pure compounds. It is often employed in pharmaceutical research and development to produce chiral intermediates or active pharmaceutical ingredients (APIs) with high enantioselectivity. Additionally, it finds application in materials science for the development of advanced chiral materials, such as liquid crystals or polymers with specific optical properties. Its role in enhancing the efficiency and selectivity of chemical processes makes it a valuable tool in both academic and industrial settings.

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