(4R,4'R,5S,5'S)-2,2'-(1-Methylethylidene)bis[4,5-dihydro-4,5-diphenyloxazole]

≥98%,99%e.e.

Reagent Code: #59711
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CAS Number 157904-67-1

science Other reagents with same CAS 157904-67-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 486.6 g/mol
Formula C₃₃H₃₀N₂O₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce enantiomerically pure compounds, which are essential in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs). Its robust structure and ability to induce high enantioselectivity make it valuable in the development of drugs, agrochemicals, and fine chemicals. Additionally, it is used in academic and industrial research to explore new catalytic methodologies and optimize existing synthetic routes.

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Test Parameter Specification
Appearance White to yellow to beige to brown powder or crystals or solids
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 ฿12,740.00
inventory 100mg
10-20 days ฿5,913.00

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(4R,4'R,5S,5'S)-2,2'-(1-Methylethylidene)bis[4,5-dihydro-4,5-diphenyloxazole]
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This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce enantiomerically pure compounds, which are essential in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs). Its robust structure and ability to induce high enantioselectivity make it valuable in the development of drugs,

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce enantiomerically pure compounds, which are essential in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs). Its robust structure and ability to induce high enantioselectivity make it valuable in the development of drugs, agrochemicals, and fine chemicals. Additionally, it is used in academic and industrial research to explore new catalytic methodologies and optimize existing synthetic routes.

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