(S)-6,6'-Dibromo-2,2'-bis(methoxymethoxy)-1,1'-binaphthalene

≥98%,99%e.e.

Reagent Code: #65654
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CAS Number 211560-97-3

science Other reagents with same CAS 211560-97-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 532.2 g/mol
Formula C₂₄H₂₀Br₂O₄
thermostat Physical Properties
Boiling Point 553.0±50.0 °C
inventory_2 Storage & Handling
Density 1.524±0.06 g/mL
Storage room temperature, dry

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is effective in facilitating the formation of chiral centers in organic molecules, making it valuable in the production of pharmaceuticals and fine chemicals. Additionally, it serves as a key component in the development of advanced materials, such as chiral polymers or liquid crystals, which require precise stereochemical control. Its unique structure and properties make it suitable for applications in organic electronics and optoelectronics, where chiral materials are essential for performance optimization.

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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 250mg
10-20 days ฿1,680.00
inventory 1g
10-20 days ฿4,790.00
inventory 5g
10-20 days ฿18,590.00

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(S)-6,6'-Dibromo-2,2'-bis(methoxymethoxy)-1,1'-binaphthalene
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This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is effective in facilitating the formation of chiral centers in organic molecules, making it valuable in the production of pharmaceuticals and fine chemicals. Additionally, it serves as a key component in the development of advanced materials, such as chiral polymers or liquid crystals, which require precise stereochemical control. Its unique structure an

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is effective in facilitating the formation of chiral centers in organic molecules, making it valuable in the production of pharmaceuticals and fine chemicals. Additionally, it serves as a key component in the development of advanced materials, such as chiral polymers or liquid crystals, which require precise stereochemical control. Its unique structure and properties make it suitable for applications in organic electronics and optoelectronics, where chiral materials are essential for performance optimization.

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