(S)-α,α-Bis[3,5-bis(trifluoromethyl)phenyl]-2-pyrrolidinemethanol trimethylsilyl ether

95%

Reagent Code: #62367
label
Alias (S)-2-[(bis(3,5-bis(trifluoromethyl)phenyl)trimethylsilyloxy)methyl]pyrrolidine
fingerprint
CAS Number 848821-61-4

science Other reagents with same CAS 848821-61-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 597.51 g/mol
Formula C₂₄H₂₃F₁₂NOSi
badge Registry Numbers
MDL Number MFCD09750447
thermostat Physical Properties
Melting Point 48-56 °C
inventory_2 Storage & Handling
Storage 2~8℃, dry

description Product Description

This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in the pharmaceutical industry. It serves as a chiral ligand or catalyst in various enantioselective reactions, such as hydrogenation, alkylation, and cycloaddition processes. Its trifluoromethyl groups enhance its electron-withdrawing properties, making it effective in stabilizing transition states and improving reaction selectivity. Additionally, the trimethylsilyl ether group provides steric protection and enhances solubility in organic solvents, facilitating its use in complex synthetic pathways. Its application is critical in the production of chiral intermediates for active pharmaceutical ingredients (APIs), ensuring high enantiomeric purity in the final products.

format_list_bulleted Product Specification

Test Parameter Specification
Melting point 48-56
Purity 95-100%
Appearance White crystal powder
Note Low melting point solid, may change state in different environments (solid, liquid or semi-solid)

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿11,860.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-α,α-Bis[3,5-bis(trifluoromethyl)phenyl]-2-pyrrolidinemethanol trimethylsilyl ether
No image available

This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in the pharmaceutical industry. It serves as a chiral ligand or catalyst in various enantioselective reactions, such as hydrogenation, alkylation, and cycloaddition processes. Its trifluoromethyl groups enhance its electron-withdrawing properties, making it effective in stabilizing transition states and improving reaction selectivity. Additionally, the trimethylsilyl ether group provides steric protection and enhances

This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in the pharmaceutical industry. It serves as a chiral ligand or catalyst in various enantioselective reactions, such as hydrogenation, alkylation, and cycloaddition processes. Its trifluoromethyl groups enhance its electron-withdrawing properties, making it effective in stabilizing transition states and improving reaction selectivity. Additionally, the trimethylsilyl ether group provides steric protection and enhances solubility in organic solvents, facilitating its use in complex synthetic pathways. Its application is critical in the production of chiral intermediates for active pharmaceutical ingredients (APIs), ensuring high enantiomeric purity in the final products.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...