(2-fluoro-6-(piperidin-4-yl)pyridin-3-yl)boronic acid

95%

Reagent Code: #58137
fingerprint
CAS Number 2225180-58-3

science Other reagents with same CAS 2225180-58-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.0397632 g/mol
Formula C₁₀H₁₄BFN₂O₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly in the synthesis of complex molecules. It serves as a key intermediate in the creation of biologically active compounds, especially those targeting neurological disorders and cancers. Its boronic acid group facilitates Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds essential for constructing diverse pharmaceutical agents. Additionally, the piperidine moiety enhances the compound's ability to interact with biological targets, making it valuable in the design of receptor-specific drugs. Its fluorine atom further contributes to metabolic stability and binding affinity, enhancing its efficacy in therapeutic applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿47,800.00
inventory 25mg
10-20 days ฿133,300.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(2-fluoro-6-(piperidin-4-yl)pyridin-3-yl)boronic acid
No image available

This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly in the synthesis of complex molecules. It serves as a key intermediate in the creation of biologically active compounds, especially those targeting neurological disorders and cancers. Its boronic acid group facilitates Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds essential for constructing diverse pharmaceutical agents. Additionally, the piperidine moiety en

This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly in the synthesis of complex molecules. It serves as a key intermediate in the creation of biologically active compounds, especially those targeting neurological disorders and cancers. Its boronic acid group facilitates Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds essential for constructing diverse pharmaceutical agents. Additionally, the piperidine moiety enhances the compound's ability to interact with biological targets, making it valuable in the design of receptor-specific drugs. Its fluorine atom further contributes to metabolic stability and binding affinity, enhancing its efficacy in therapeutic applications.

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...