(2R)-2-[[[(1,1-Dimethylethyl)dimethylsilyl]oxy]diphenylmethyl]pyrrolidine

≥95%,99%e.e.

Reagent Code: #70410
fingerprint
CAS Number 1236033-34-3

science Other reagents with same CAS 1236033-34-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 367.6 g/mol
Formula C₂₃H₃₃NOSi
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily used in organic synthesis, particularly in the field of asymmetric catalysis and chiral resolution. It serves as a key intermediate in the preparation of complex molecules, including pharmaceuticals, where stereochemistry plays a crucial role. Its structure, featuring a silyl-protected hydroxyl group and a diphenylmethyl moiety, makes it valuable for protecting functional groups during multi-step synthetic processes. Additionally, it is employed in the synthesis of chiral ligands, which are essential for creating enantioselective catalysts used in producing optically active compounds. Its application extends to the development of novel drugs and fine chemicals, where precise control over molecular configuration is required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿9,900.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(2R)-2-[[[(1,1-Dimethylethyl)dimethylsilyl]oxy]diphenylmethyl]pyrrolidine
No image available

This compound is primarily used in organic synthesis, particularly in the field of asymmetric catalysis and chiral resolution. It serves as a key intermediate in the preparation of complex molecules, including pharmaceuticals, where stereochemistry plays a crucial role. Its structure, featuring a silyl-protected hydroxyl group and a diphenylmethyl moiety, makes it valuable for protecting functional groups during multi-step synthetic processes. Additionally, it is employed in the synthesis of chiral ligan

This compound is primarily used in organic synthesis, particularly in the field of asymmetric catalysis and chiral resolution. It serves as a key intermediate in the preparation of complex molecules, including pharmaceuticals, where stereochemistry plays a crucial role. Its structure, featuring a silyl-protected hydroxyl group and a diphenylmethyl moiety, makes it valuable for protecting functional groups during multi-step synthetic processes. Additionally, it is employed in the synthesis of chiral ligands, which are essential for creating enantioselective catalysts used in producing optically active compounds. Its application extends to the development of novel drugs and fine chemicals, where precise control over molecular configuration is required.

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...