2-(2,3-Dihydrobenzofuran-6-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

95%

Reagent Code: #171513
fingerprint
CAS Number 445303-12-8

science Other reagents with same CAS 445303-12-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.11 g/mol
Formula C₁₄H₁₉BO₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates palladium-catalyzed coupling with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research for constructing biaryl frameworks. The dihydrobenzofuran moiety contributes to the development of bioactive compounds, including those with potential neurological or anti-inflammatory activity. Commonly employed in medicinal chemistry for lead optimization and library synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,050.00
inventory 250mg
10-20 days ฿1,970.00
inventory 1g
10-20 days ฿7,560.00
inventory 5g
10-20 days ฿31,330.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-(2,3-Dihydrobenzofuran-6-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 the synthesis of complex organic molecules. Its boronate ester group facilitates palladium-catalyzed coupling with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research for constructing biaryl frameworks. The dihydrobenzofuran moiety contributes to the development of bioactive compounds, including those with potential neurological or anti-inflammatory act

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates palladium-catalyzed coupling with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research for constructing biaryl frameworks. The dihydrobenzofuran moiety contributes to the development of bioactive compounds, including those with potential neurological or anti-inflammatory activity. Commonly employed in medicinal chemistry for lead optimization and library synthesis.

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...