(R)-6,6'-Dibromo-2,2',3,3'-tetrahydro-1,1'-spirobi[indene]-7,7'-diol

≥98%,99%e.e.

Reagent Code: #84849
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CAS Number 1286189-15-8

science Other reagents with same CAS 1286189-15-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 410.10 g/mol
Formula C₁₇H₁₄Br₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This chemical is primarily utilized in the synthesis of chiral ligands and catalysts, which are essential in asymmetric organic synthesis. Its unique spirobiindene structure and hydroxyl groups make it a valuable building block for creating complex molecules with high enantioselectivity. It is often employed in the development of pharmaceuticals, where precise stereochemistry is crucial for the efficacy and safety of drugs. Additionally, it finds applications in material science, particularly in the design of chiral polymers and advanced materials with specific optical properties. Its role in facilitating stereocontrolled reactions makes it a key component in research and industrial processes aimed at producing enantiomerically pure compounds.

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Test Parameter Specification
Appearance White to brown solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿3,600.00
inventory 100mg
10-20 days ฿8,690.00
inventory 500mg
10-20 days ฿28,960.00

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(R)-6,6'-Dibromo-2,2',3,3'-tetrahydro-1,1'-spirobi[indene]-7,7'-diol
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This chemical is primarily utilized in the synthesis of chiral ligands and catalysts, which are essential in asymmetric organic synthesis. Its unique spirobiindene structure and hydroxyl groups make it a valuable building block for creating complex molecules with high enantioselectivity. It is often employed in the development of pharmaceuticals, where precise stereochemistry is crucial for the efficacy and safety of drugs. Additionally, it finds applications in material science, particularly in the desi

This chemical is primarily utilized in the synthesis of chiral ligands and catalysts, which are essential in asymmetric organic synthesis. Its unique spirobiindene structure and hydroxyl groups make it a valuable building block for creating complex molecules with high enantioselectivity. It is often employed in the development of pharmaceuticals, where precise stereochemistry is crucial for the efficacy and safety of drugs. Additionally, it finds applications in material science, particularly in the design of chiral polymers and advanced materials with specific optical properties. Its role in facilitating stereocontrolled reactions makes it a key component in research and industrial processes aimed at producing enantiomerically pure compounds.

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