R-3,3'-diiodo-[1,1'-Binaphthalene]-2,2'-diol

98%, ee 99%

Reagent Code: #55386
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CAS Number 287111-93-7

science Other reagents with same CAS 287111-93-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 538.11702 g/mol
Formula C₂₀H₁₂I₂O₂
badge Registry Numbers
MDL Number MFCD25372833
thermostat Physical Properties
Melting Point 312-314 °C
Boiling Point 491.7±45.0 °C
inventory_2 Storage & Handling
Density 2.038±0.06 g/cm3(Predicted)
Storage room temperature

description Product Description

This chemical is primarily utilized in asymmetric synthesis and catalysis, where it serves as a chiral ligand or catalyst in various organic reactions. Its binaphthyl structure and iodine substituents make it effective in promoting enantioselective transformations, such as the synthesis of chiral alcohols, amines, and other optically active compounds. It is particularly valuable in pharmaceutical research for creating enantiomerically pure drugs. Additionally, it finds use in material science for developing chiral polymers and frameworks with specific optical properties. Its stability and unique steric properties make it a versatile tool in advanced chemical synthesis.

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Test Parameter Specification
Appearance Yellow Powder
Purity (%) 97.5-100%
ee (%) 98.5-100%
Specific Rotation [A]20/D (c=1, THF) 100.96-106.96
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100 mg
10-20 days ฿690.00
inventory 1 g
10-20 days ฿4,670.00
inventory 500 mg
10-20 days ฿2,480.00

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R-3,3'-diiodo-[1,1'-Binaphthalene]-2,2'-diol
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This chemical is primarily utilized in asymmetric synthesis and catalysis, where it serves as a chiral ligand or catalyst in various organic reactions. Its binaphthyl structure and iodine substituents make it effective in promoting enantioselective transformations, such as the synthesis of chiral alcohols, amines, and other optically active compounds. It is particularly valuable in pharmaceutical research for creating enantiomerically pure drugs. Additionally, it finds use in material science for developing chiral polymers and frameworks with specific optical properties. Its stability and unique steric properties make it a versatile tool in advanced chemical synthesis.
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