4-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

≥95%

Reagent Code: #116175
fingerprint
CAS Number 1398923-95-9

science Other reagents with same CAS 1398923-95-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.06 g/mol
Formula C₁₂H₁₆BFO₃
badge Registry Numbers
MDL Number MFCD16994432
thermostat Physical Properties
Boiling Point 354.1°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceuticals and agrochemicals. Its boronate ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the development of advanced materials, such as organic semiconductors and polymers, due to its ability to introduce fluorine and phenol functionalities into molecular structures. Its applications also extend to medicinal chemistry, where it is used to create bioactive compounds with potential therapeutic properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿20,412.00
inventory 250mg
10-20 days ฿1,080.00
inventory 1g
10-20 days ฿4,212.00
inventory 100mg
10-20 days ฿747.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
No image available

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceuticals and agrochemicals. Its boronate ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the development of advanced materials, such as organic semiconductors and polymers, due to its a

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceuticals and agrochemicals. Its boronate ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the development of advanced materials, such as organic semiconductors and polymers, due to its ability to introduce fluorine and phenol functionalities into molecular structures. Its applications also extend to medicinal chemistry, where it is used to create bioactive compounds with potential therapeutic properties.

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...