4-(1-(4-(2-((tert-butyldiphenylsilyl)oxy)ethyl)piperazin-1-yl)ethyl)phenyl)boronic acid

98%

Reagent Code: #90317
fingerprint
CAS Number 1704082-49-4

science Other reagents with same CAS 1704082-49-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 516.5700000000001 g/mol
Formula C₃₀H₄₁BN₂O₃Si
badge Registry Numbers
MDL Number MFCD28805777
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic acid coupling partner. Its structure, featuring a piperazine ring and a tert-butyldiphenylsilyl (TBDPS) protecting group, makes it valuable in the synthesis of complex molecules, including pharmaceuticals and bioactive compounds. The TBDPS group provides stability during reactions, allowing selective deprotection when needed. Additionally, its boronic acid moiety enables the formation of carbon-carbon bonds, making it essential in constructing diverse organic frameworks. This chemical is often employed in medicinal chemistry for the development of drug candidates, particularly in targeting specific biological pathways or receptors. Its versatility and functional groups make it a useful intermediate in multi-step synthetic processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿39,330.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-(1-(4-(2-((tert-butyldiphenylsilyl)oxy)ethyl)piperazin-1-yl)ethyl)phenyl)boronic acid
No image available
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic acid coupling partner. Its structure, featuring a piperazine ring and a tert-butyldiphenylsilyl (TBDPS) protecting group, makes it valuable in the synthesis of complex molecules, including pharmaceuticals and bioactive compounds. The TBDPS group provides stability during reactions, allowing selective deprotection when needed. Additionally, its boronic acid moiety enables the formation of carbon-carbon bonds, making it essential in constructing diverse organic frameworks. This chemical is often employed in medicinal chemistry for the development of drug candidates, particularly in targeting specific biological pathways or receptors. Its versatility and functional groups make it a useful intermediate in multi-step synthetic processes.
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...