2-(3,5-Difluoro-4-propoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

95%

Reagent Code: #130989
fingerprint
CAS Number 2828445-55-0

science Other reagents with same CAS 2828445-55-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 298.13 g/mol
Formula C₁₅H₂₁BF₂O₃
badge Registry Numbers
MDL Number MFCD33403760
thermostat Physical Properties
Boiling Point 362.7±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.10±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

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 in the development of new drug candidates and functional materials. The presence of fluorine and propoxy substituents enhances electronic and metabolic stability in target compounds, which is advantageous in medicinal chemistry applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿10,890.00
inventory 250mg
10-20 days ฿3,730.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-(3,5-Difluoro-4-propoxyphenyl)-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 in the development of new drug candidates and functional materials. The presence of fluorine and propoxy substituents enhances electronic and metabolic stability in target compounds, which is advantageous in m

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 in the development of new drug candidates and functional materials. The presence of fluorine and propoxy substituents enhances electronic and metabolic stability in target compounds, which is advantageous in medicinal chemistry applications.

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...