2-(2-fluoro-4-(methylsulfonyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

95%

Reagent Code: #131106
fingerprint
CAS Number 1384951-71-6

science Other reagents with same CAS 1384951-71-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 300.15 g/mol
Formula C₁₃H₁₈BFO₄S
badge Registry Numbers
MDL Number MFCD18760181
thermostat Physical Properties
Boiling Point 422.8±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.22±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions, making it valuable for constructing biaryl structures found in bioactive compounds. Commonly employed in late-stage functionalization due to its stability and reactivity profile.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿11,590.00
inventory 1g
10-20 days ฿30,100.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-(2-fluoro-4-(methylsulfonyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
No image available
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions, making it valuable for constructing biaryl structures found in bioactive compounds. Commonly employed in late-stage functionalization due to its stability and reactivity profile.
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...