(R)-2,2'-Dimethoxy-3,3'-diphenyl-1,1'-binaphthalene

≥98%,99%e.e.

Reagent Code: #70290
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CAS Number 219757-68-3

science Other reagents with same CAS 219757-68-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 466.6 g/mol
Formula C₃₄H₂₆O₂
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 such as hydrogenation, oxidation, and carbon-carbon bond formation. Its ability to induce chirality in products makes it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it serves as a key component in the development of chiral catalysts for enantioselective transformations, enhancing the efficiency and selectivity of synthetic processes. Its application extends to materials science, where it contributes to the creation of chiral polymers and advanced functional materials.

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Test Parameter Specification
Appearance yellow powder
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿39,860.00
inventory 100mg
10-20 days ฿7,450.00
inventory 500mg
10-20 days ฿21,360.00

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(R)-2,2'-Dimethoxy-3,3'-diphenyl-1,1'-binaphthalene
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This chemical is widely used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions such as hydrogenation, oxidation, and carbon-carbon bond formation. Its ability to induce chirality in products makes it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it serves as a key component in the development of chiral catalysts for enantioselective transformations, enhancing the efficiency and selectivity of synthetic processes. Its applicat

This chemical is widely used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions such as hydrogenation, oxidation, and carbon-carbon bond formation. Its ability to induce chirality in products makes it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it serves as a key component in the development of chiral catalysts for enantioselective transformations, enhancing the efficiency and selectivity of synthetic processes. Its application extends to materials science, where it contributes to the creation of chiral polymers and advanced functional materials.

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