(4-(2-(4-((tert-Butyldiphenylsilyl)oxy)piperidin- 1-yl)ethoxy)-3-fluorophenyl)boronic acid

98%

Reagent Code: #89230
fingerprint
CAS Number 1704082-87-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 521.5 g/mol
Formula C₂₉H₃₇BFNO₄Si
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. The tert-butyldiphenylsilyl (TBDPS) group serves as a protective moiety for hydroxyl groups, ensuring selective reactivity during multi-step synthetic processes. Its application is significant in pharmaceutical research, where it aids in the development of drug candidates by facilitating the synthesis of biologically active compounds. Additionally, the fluorine atom in its structure can enhance the metabolic stability and binding affinity of the resulting molecules, making it useful in designing more effective therapeutic agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days £141.68
(4-(2-(4-((tert-Butyldiphenylsilyl)oxy)piperidin- 1-yl)ethoxy)-3-fluorophenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. The tert-butyldiphenylsilyl (TBDPS) group serves as a protective moiety for hydroxyl groups, ensuring selective reactivity during multi-step synthetic processes. Its application is significant in pharmaceutical research, where it aids in the development of drug candidates by facilitating the synthesis of biologically active compounds. Additionally, the fluorine atom in its structure can enhance the metabolic stability and binding affinity of the resulting molecules, making it useful in designing more effective therapeutic agents.
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...

Cart

No products

Subtotal: £0.00
Total £0.00 GBP