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

97%

Reagent Code: #119875
fingerprint
CAS Number 1038828-32-8

science Other reagents with same CAS 1038828-32-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.06 g/mol
Formula C₁₂H₁₆BFO₃
badge Registry Numbers
MDL Number MFCD16994248
thermostat Physical Properties
Boiling Point 320.4±32.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for the preparation of complex molecules, including pharmaceuticals and agrochemicals. Its boronate ester group enables efficient coupling with aryl or vinyl halides, facilitating the construction of carbon-carbon bonds. Additionally, it is employed in the development of advanced materials, including polymers and organic electronic components. The fluorine substituent enhances its reactivity and selectivity in various chemical transformations, making it valuable in medicinal chemistry for drug discovery and development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿14,840.00
inventory 100mg
10-20 days ฿3,200.00
inventory 250mg
10-20 days ฿7,840.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
5-Fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
No image available
This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for the preparation of complex molecules, including pharmaceuticals and agrochemicals. Its boronate ester group enables efficient coupling with aryl or vinyl halides, facilitating the construction of carbon-carbon bonds. Additionally, it is employed in the development of advanced materials, including polymers and organic electronic components. The fluorine substituent enhances its reactivity and selectivity in various chemical transformations, making it valuable in medicinal chemistry for drug discovery and development.
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...