(S)-7,7-Bis[(4S)-(phenyl)oxazol-2-yl)]-2,2,3,3-tetrahydro-1,1-spirobiindane

98%

Reagent Code: #59724
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CAS Number 940880-69-3

science Other reagents with same CAS 940880-69-3

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scatter_plot Molecular Information
Weight 510.62 g/mol
Formula C₃₅H₃₀N₂O₂
badge Registry Numbers
MDL Number MFCD17018767
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in asymmetric catalysis, particularly in enantioselective synthesis, where it serves as a chiral ligand. Its unique spirobiindane structure and oxazole groups enable it to effectively coordinate with metal centers, such as rhodium or iridium, to facilitate highly selective reactions. This makes it valuable in the production of pharmaceuticals, where precise stereochemistry is crucial for drug efficacy and safety. Additionally, it is employed in the synthesis of complex organic molecules, including natural products and fine chemicals, where its ability to induce high enantiomeric excess is highly advantageous. Its application extends to academic research, where it is used to develop new catalytic methodologies and explore chiral induction mechanisms.

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inventory 50mg
10-20 days ฿13,950.00

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(S)-7,7-Bis[(4S)-(phenyl)oxazol-2-yl)]-2,2,3,3-tetrahydro-1,1-spirobiindane
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This chemical is primarily utilized in asymmetric catalysis, particularly in enantioselective synthesis, where it serves as a chiral ligand. Its unique spirobiindane structure and oxazole groups enable it to effectively coordinate with metal centers, such as rhodium or iridium, to facilitate highly selective reactions. This makes it valuable in the production of pharmaceuticals, where precise stereochemistry is crucial for drug efficacy and safety. Additionally, it is employed in the synthesis of complex

This chemical is primarily utilized in asymmetric catalysis, particularly in enantioselective synthesis, where it serves as a chiral ligand. Its unique spirobiindane structure and oxazole groups enable it to effectively coordinate with metal centers, such as rhodium or iridium, to facilitate highly selective reactions. This makes it valuable in the production of pharmaceuticals, where precise stereochemistry is crucial for drug efficacy and safety. Additionally, it is employed in the synthesis of complex organic molecules, including natural products and fine chemicals, where its ability to induce high enantiomeric excess is highly advantageous. Its application extends to academic research, where it is used to develop new catalytic methodologies and explore chiral induction mechanisms.

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