(S)​-2-​[Bis[3,​5-​bis(trifluoromethyl)​phenyl]​[[trisisopropylsilyl]​oxy]​methyl]​pyrrolidine

≥98%,99%e.e.

Reagent Code: #65695
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CAS Number 1415760-15-4

science Other reagents with same CAS 1415760-15-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 681.7 g/mol
Formula C₃₀H₃₅F₁₂NOSi
thermostat Physical Properties
Boiling Point 456.5±40.0 °C
inventory_2 Storage & Handling
Density 1.233±0.06 g/mL
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in asymmetric synthesis, particularly in the field of organic chemistry, where it serves as a chiral catalyst or ligand. Its unique structure, featuring trifluoromethyl groups and a trisopropylsilyloxy moiety, enhances its ability to induce stereoselectivity in various reactions, such as enantioselective hydrogenation, aldol reactions, and Michael additions. The compound is often employed in the synthesis of complex molecules, including pharmaceuticals and fine chemicals, where precise control over chirality is critical. Its robustness and efficiency make it a valuable tool in the development of enantiomerically pure compounds, which are essential in drug discovery and manufacturing.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,210.00

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(S)​-2-​[Bis[3,​5-​bis(trifluoromethyl)​phenyl]​[[trisisopropylsilyl]​oxy]​methyl]​pyrrolidine
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This chemical is primarily utilized in asymmetric synthesis, particularly in the field of organic chemistry, where it serves as a chiral catalyst or ligand. Its unique structure, featuring trifluoromethyl groups and a trisopropylsilyloxy moiety, enhances its ability to induce stereoselectivity in various reactions, such as enantioselective hydrogenation, aldol reactions, and Michael additions. The compound is often employed in the synthesis of complex molecules, including pharmaceuticals and fine chemica

This chemical is primarily utilized in asymmetric synthesis, particularly in the field of organic chemistry, where it serves as a chiral catalyst or ligand. Its unique structure, featuring trifluoromethyl groups and a trisopropylsilyloxy moiety, enhances its ability to induce stereoselectivity in various reactions, such as enantioselective hydrogenation, aldol reactions, and Michael additions. The compound is often employed in the synthesis of complex molecules, including pharmaceuticals and fine chemicals, where precise control over chirality is critical. Its robustness and efficiency make it a valuable tool in the development of enantiomerically pure compounds, which are essential in drug discovery and manufacturing.

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