(R)-3,3'-Bis(2,4,6-triisopropylphenyl)-1,1'-bi-2-naphthol

≥98%,99%e.e.

Reagent Code: #70312
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CAS Number 247123-09-7

science Other reagents with same CAS 247123-09-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 691 g/mol
Formula C₅₀H₅₈O₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is widely used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is employed in the development of pharmaceuticals, agrochemicals, and fine chemicals, enabling the production of enantiomerically pure compounds. Additionally, it serves as a key component in asymmetric hydrogenation, carbon-carbon bond formation, and other stereoselective transformations, enhancing the efficiency and precision of these processes. Its robust structure and steric properties make it highly effective in controlling the stereochemistry of complex organic reactions.

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

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿37,380.00
inventory 100mg
10-20 days ฿14,418.00

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(R)-3,3'-Bis(2,4,6-triisopropylphenyl)-1,1'-bi-2-naphthol
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This chemical is widely used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is employed in the development of pharmaceuticals, agrochemicals, and fine chemicals, enabling the production of enantiomerically pure compounds. Additionally, it serves as a key component in asymmetric hydrogenation, carbon-carbon bond formation, and other stereoselective transformations, enhancing the efficiency and precision of these processes. Its

This chemical is widely used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is employed in the development of pharmaceuticals, agrochemicals, and fine chemicals, enabling the production of enantiomerically pure compounds. Additionally, it serves as a key component in asymmetric hydrogenation, carbon-carbon bond formation, and other stereoselective transformations, enhancing the efficiency and precision of these processes. Its robust structure and steric properties make it highly effective in controlling the stereochemistry of complex organic reactions.

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