2,6-Bis[(2S,4S)-4-methyl-5,5-diphenyloxazolidin-2-yl]pyridine

Reagent Code: #69833
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CAS Number 1450841-25-4

science Other reagents with same CAS 1450841-25-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 553.71 g/mol
Formula C₃₇H₃₅N₃O₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Used as a chiral ligand in asymmetric synthesis, it facilitates the formation of enantiomerically pure compounds, which are crucial in the production of pharmaceuticals and fine chemicals. Its application extends to catalyzing stereoselective reactions, such as aldol additions and Diels-Alder reactions, ensuring high enantioselectivity and yield. This makes it valuable in the development of drugs and bioactive molecules with specific stereochemical requirements. Additionally, it is employed in academic research to study and optimize asymmetric catalytic processes.

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Test Parameter Specification
Appearance White to light yellow powder to crystal
Elemental Analysis (Nitrogen) 7-8%
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿3,980.00

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2,6-Bis[(2S,4S)-4-methyl-5,5-diphenyloxazolidin-2-yl]pyridine
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Used as a chiral ligand in asymmetric synthesis, it facilitates the formation of enantiomerically pure compounds, which are crucial in the production of pharmaceuticals and fine chemicals. Its application extends to catalyzing stereoselective reactions, such as aldol additions and Diels-Alder reactions, ensuring high enantioselectivity and yield. This makes it valuable in the development of drugs and bioactive molecules with specific stereochemical requirements. Additionally, it is employed in academic r

Used as a chiral ligand in asymmetric synthesis, it facilitates the formation of enantiomerically pure compounds, which are crucial in the production of pharmaceuticals and fine chemicals. Its application extends to catalyzing stereoselective reactions, such as aldol additions and Diels-Alder reactions, ensuring high enantioselectivity and yield. This makes it valuable in the development of drugs and bioactive molecules with specific stereochemical requirements. Additionally, it is employed in academic research to study and optimize asymmetric catalytic processes.

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