(R)-6,6'-Bis(3,5-dimethylphenyl)-2,2',3,3'-tetrahydro-1,1'-spirobi[1H-indene]-7,7'-diol

≥98%,99%e.e.

Reagent Code: #70378
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CAS Number 930784-56-8

science Other reagents with same CAS 930784-56-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 460.6 g/mol
Formula C₃₃H₃₂O₂
thermostat Physical Properties
Melting Point 93-94°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. It serves as a key ligand in transition metal-catalyzed reactions, enabling the production of enantiomerically pure pharmaceuticals and fine chemicals. Its unique structure enhances selectivity and efficiency in processes such as hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. Additionally, it is employed in the development of advanced materials and as a chiral resolving agent in organic synthesis. Its applications are critical in industries requiring high-precision molecular control, such as drug manufacturing and specialty chemical production.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿31,430.00

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(R)-6,6'-Bis(3,5-dimethylphenyl)-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. It serves as a key ligand in transition metal-catalyzed reactions, enabling the production of enantiomerically pure pharmaceuticals and fine chemicals. Its unique structure enhances selectivity and efficiency in processes such as hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. Additionally, it is employed in the development of advanced materials and as a c

This chemical is primarily utilized in asymmetric catalysis, particularly in the synthesis of chiral compounds. It serves as a key ligand in transition metal-catalyzed reactions, enabling the production of enantiomerically pure pharmaceuticals and fine chemicals. Its unique structure enhances selectivity and efficiency in processes such as hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. Additionally, it is employed in the development of advanced materials and as a chiral resolving agent in organic synthesis. Its applications are critical in industries requiring high-precision molecular control, such as drug manufacturing and specialty chemical production.

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