(R)-2-(Bis(3,5-bis(trifluoromethyl)phenyl)((triethylsilyl)oxy)methyl)pyrrolidine

98%

Reagent Code: #51897
fingerprint
CAS Number 1061307-56-9

science Other reagents with same CAS 1061307-56-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 639.5900 g/mol
Formula C₂₇H₂₉F₁₂NOSi
badge Registry Numbers
MDL Number MFCD27975624
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in asymmetric synthesis, particularly as a chiral catalyst or ligand in organic reactions. Its unique structure, featuring trifluoromethyl groups and a triethylsilyl moiety, enhances its steric and electronic properties, making it highly effective in enantioselective transformations. It is often employed in the synthesis of complex molecules, including pharmaceuticals, where precise control over stereochemistry is crucial. Additionally, its stability and reactivity under various conditions make it a valuable tool in the development of new synthetic methodologies, especially in the formation of carbon-carbon and carbon-heteroatom bonds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,380.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-2-(Bis(3,5-bis(trifluoromethyl)phenyl)((triethylsilyl)oxy)methyl)pyrrolidine
No image available

This compound is primarily utilized in asymmetric synthesis, particularly as a chiral catalyst or ligand in organic reactions. Its unique structure, featuring trifluoromethyl groups and a triethylsilyl moiety, enhances its steric and electronic properties, making it highly effective in enantioselective transformations. It is often employed in the synthesis of complex molecules, including pharmaceuticals, where precise control over stereochemistry is crucial. Additionally, its stability and reactivity und

This compound is primarily utilized in asymmetric synthesis, particularly as a chiral catalyst or ligand in organic reactions. Its unique structure, featuring trifluoromethyl groups and a triethylsilyl moiety, enhances its steric and electronic properties, making it highly effective in enantioselective transformations. It is often employed in the synthesis of complex molecules, including pharmaceuticals, where precise control over stereochemistry is crucial. Additionally, its stability and reactivity under various conditions make it a valuable tool in the development of new synthetic methodologies, especially in the formation of carbon-carbon and carbon-heteroatom bonds.

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...