2-3-[(4-bromo-2-fluorophenoxy)methyl]phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

95%

Reagent Code: #41444
fingerprint
CAS Number 2246736-67-2

science Other reagents with same CAS 2246736-67-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 407.0816432 g/mol
Formula C₁₉H₂₁BBrFO₃
badge Registry Numbers
MDL Number MFCD31916481
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of more complex molecules, particularly in the field of pharmaceuticals and agrochemicals. Its boronic ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in the development of drugs, enabling the creation of diverse aromatic compounds with potential therapeutic properties. Additionally, its specific structure, containing a bromo and fluoro substituent, allows for further functionalization, making it a versatile building block in medicinal chemistry research. It is also explored in material science for the synthesis of advanced organic materials, particularly those requiring precise molecular architectures.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿22,500.00
inventory 250mg
10-20 days ฿7,785.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-3-[(4-bromo-2-fluorophenoxy)methyl]phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
No image available

This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of more complex molecules, particularly in the field of pharmaceuticals and agrochemicals. Its boronic ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in the development of drugs, enabling the creation of diverse aromatic compounds with potential therapeutic properties. Additionally, its spec

This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of more complex molecules, particularly in the field of pharmaceuticals and agrochemicals. Its boronic ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in the development of drugs, enabling the creation of diverse aromatic compounds with potential therapeutic properties. Additionally, its specific structure, containing a bromo and fluoro substituent, allows for further functionalization, making it a versatile building block in medicinal chemistry research. It is also explored in material science for the synthesis of advanced organic materials, particularly those requiring precise molecular architectures.

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...