4-ethoxy-2,6-difluorophenylboronic acid

≥95%

Reagent Code: #181998
fingerprint
CAS Number 1310403-94-1

science Other reagents with same CAS 1310403-94-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.96 g/mol
Formula C₈H₉BF₂O₃
badge Registry Numbers
MDL Number MFCD12026735
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the development of complex fluorinated compounds. The presence of fluorine atoms and an ethoxy group enhances electronic and metabolic stability, which is advantageous in drug design. Commonly employed in the preparation of bioactive molecules and functional materials requiring tailored aromatic structures.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿880.00
inventory 1g
10-20 days ฿2,360.00
inventory 5g
10-20 days ฿9,240.00
inventory 25g
10-20 days ฿29,860.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-ethoxy-2,6-difluorophenylboronic acid
No image available

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the development of complex fluorinated compounds. The presence of fluorine atoms and an ethoxy group enhances electronic and metabolic stability, which is advantageous in drug design. Commonly employed in the preparation of bioactive molecules and

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the development of complex fluorinated compounds. The presence of fluorine atoms and an ethoxy group enhances electronic and metabolic stability, which is advantageous in drug design. Commonly employed in the preparation of bioactive molecules and functional materials requiring tailored aromatic structures.

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...