(S)-6,6'-Bis[3,5-bis(trifluoromethyl)phenyl]-2,2',3,3'-tetrahydro-1,1'-spirobi[1H-indene]-7,7'-diol

≥98%,99%e.e.

Reagent Code: #65653
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CAS Number 1258327-01-3

science Other reagents with same CAS 1258327-01-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 676.5 g/mol
Formula C₃₃H₂₀F₁₂O₂
thermostat Physical Properties
Melting Point 205-206°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in asymmetric catalysis, particularly in the synthesis of chiral compounds. Its unique structure and properties make it highly effective as a ligand in transition metal-catalyzed reactions, such as hydrogenation, carbon-carbon bond formation, and other enantioselective transformations. It is often employed in the pharmaceutical industry to produce optically active intermediates for drug development, ensuring high enantiomeric purity. Additionally, it finds application in material science for the creation of advanced chiral materials with specific optical or electronic properties. Its stability and reactivity under various conditions make it a valuable tool in organic synthesis and industrial processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿28,760.00

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(S)-6,6'-Bis[3,5-bis(trifluoromethyl)phenyl]-2,2',3,3'-tetrahydro-1,1'-spirobi[1H-indene]-7,7'-diol
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This chemical is primarily utilized in asymmetric catalysis, particularly in the synthesis of chiral compounds. Its unique structure and properties make it highly effective as a ligand in transition metal-catalyzed reactions, such as hydrogenation, carbon-carbon bond formation, and other enantioselective transformations. It is often employed in the pharmaceutical industry to produce optically active intermediates for drug development, ensuring high enantiomeric purity. Additionally, it finds application

This chemical is primarily utilized in asymmetric catalysis, particularly in the synthesis of chiral compounds. Its unique structure and properties make it highly effective as a ligand in transition metal-catalyzed reactions, such as hydrogenation, carbon-carbon bond formation, and other enantioselective transformations. It is often employed in the pharmaceutical industry to produce optically active intermediates for drug development, ensuring high enantiomeric purity. Additionally, it finds application in material science for the creation of advanced chiral materials with specific optical or electronic properties. Its stability and reactivity under various conditions make it a valuable tool in organic synthesis and industrial processes.

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