4-(4-Fluorophenyl)thiophene-2-boronic acid

95%

Reagent Code: #90430
fingerprint
CAS Number 2225169-65-1

science Other reagents with same CAS 2225169-65-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.0437232 g/mol
Formula C₁₀H₈BFO₂S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex organic compounds. It serves as a key intermediate in the production of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in constructing biaryl structures. Also employed in material science for developing organic electronic materials, such as OLEDs and conductive polymers. Its fluorophenyl group enhances stability and reactivity in various chemical processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿13,140.00
inventory 250mg
10-20 days ฿39,420.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-(4-Fluorophenyl)thiophene-2-boronic acid
No image available

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex organic compounds. It serves as a key intermediate in the production of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in constructing biaryl structures. Also employed in material science for developing organic electronic materials, such as OLEDs and conductive polymers. Its fluorophenyl group enhances stability and reactivity in

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex organic compounds. It serves as a key intermediate in the production of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in constructing biaryl structures. Also employed in material science for developing organic electronic materials, such as OLEDs and conductive polymers. Its fluorophenyl group enhances stability and reactivity in various chemical 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...