2-(2-(3-fluorophenyl)prop-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

98%

Reagent Code: #188287
fingerprint
CAS Number 1398771-28-2

science Other reagents with same CAS 1398771-28-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.13 g/mol
Formula C₁₅H₂₀BFO₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The presence of the fluorophenyl group can enhance binding affinity and metabolic stability in bioactive compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,820.00
inventory 1g
10-20 days ฿19,230.00
inventory 5g
10-20 days ฿50,010.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-(2-(3-fluorophenyl)prop-1-en-1-yl)-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 formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The presence of the fluorophenyl group can enhance binding affinity and metabolic stability in bioactive compounds.
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...