N-[2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]benzamide

95%

Reagent Code: #83841
fingerprint
CAS Number 2246744-18-1

science Other reagents with same CAS 2246744-18-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 341.1843432 g/mol
Formula C₁₉H₂₁BFNO₃
badge Registry Numbers
MDL Number MFCD32206446
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group makes it a valuable intermediate for constructing complex organic molecules, especially in pharmaceutical research and development. It is often employed in the synthesis of bioactive compounds, including potential drug candidates, due to its ability to introduce aromatic rings with specific functional groups. Additionally, it is used in material science for creating advanced polymers and organic electronic materials, where precise molecular architecture is crucial. Its fluorine substituent further enhances its utility in designing molecules with improved metabolic stability and binding affinity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿4,338.00
inventory 100mg
10-20 days ฿12,996.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
N-[2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]benzamide
No image available

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group makes it a valuable intermediate for constructing complex organic molecules, especially in pharmaceutical research and development. It is often employed in the synthesis of bioactive compounds, including potential drug candidates, due to its ability to introduce aromatic rings with specific functional groups. Additionally, it is used in material scie

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group makes it a valuable intermediate for constructing complex organic molecules, especially in pharmaceutical research and development. It is often employed in the synthesis of bioactive compounds, including potential drug candidates, due to its ability to introduce aromatic rings with specific functional groups. Additionally, it is used in material science for creating advanced polymers and organic electronic materials, where precise molecular architecture is crucial. Its fluorine substituent further enhances its utility in designing molecules with improved metabolic stability and binding affinity.

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...