3-Fluoro-5-ethoxycarbonylphenylboronic acid

98%

Reagent Code: #90176
fingerprint
CAS Number 871329-85-0

science Other reagents with same CAS 871329-85-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.98 g/mol
Formula C₉H₁₀BFO₄
badge Registry Numbers
MDL Number MFCD07363792
thermostat Physical Properties
Melting Point 146-150°C
Boiling Point 380.1°C
inventory_2 Storage & Handling
Density 1.29g/mL
Storage  2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group is essential for coupling with aryl halides, making it valuable in pharmaceutical research for developing new drugs and active pharmaceutical ingredients. Additionally, it is employed in material science for creating advanced polymers and organic electronic materials. The fluoro substituent at the 3-position introduces electronic effects that can modulate reactivity and stability, while the ethoxycarbonyl group at the 5-position enhances solubility and reactivity, making it suitable for diverse synthetic applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿10,000.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-Fluoro-5-ethoxycarbonylphenylboronic acid
No image available

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group is essential for coupling with aryl halides, making it valuable in pharmaceutical research for developing new drugs and active pharmaceutical ingredients. Additionally, it is employed in material science for creating advanced polymers and organic electron

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group is essential for coupling with aryl halides, making it valuable in pharmaceutical research for developing new drugs and active pharmaceutical ingredients. Additionally, it is employed in material science for creating advanced polymers and organic electronic materials. The fluoro substituent at the 3-position introduces electronic effects that can modulate reactivity and stability, while the ethoxycarbonyl group at the 5-position enhances solubility and reactivity, making it suitable for diverse synthetic 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...