(2-(Ethoxycarbonyl)furan-3-yl)boronic acid

97%

Reagent Code: #183534
fingerprint
CAS Number 1150114-62-7

science Other reagents with same CAS 1150114-62-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 183.95 g/mol
Formula C₇H₉BO₅
badge Registry Numbers
MDL Number MFCD12025973
thermostat Physical Properties
Boiling Point 364°C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, stored in inert gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex furan-containing molecules for pharmaceuticals and agrochemicals. Its boronic acid group facilitates carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and development of bioactive compounds. The ethoxycarbonyl group enhances stability and influences reactivity, allowing selective transformations in heterocyclic chemistry. Commonly employed in the preparation of functionalized furans used in materials science and medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,770.00
inventory 250mg
10-20 days ฿10,690.00
inventory 1g
10-20 days ฿26,760.00
$product.analytical_desc - NULL

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(2-(Ethoxycarbonyl)furan-3-yl)boronic acid
No image available

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex furan-containing molecules for pharmaceuticals and agrochemicals. Its boronic acid group facilitates carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and development of bioactive compounds. The ethoxycarbonyl group enhances stability and influences reactivity, allowing selective transformations in heterocyclic chemistry. Commonly employed in the preparation of f

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex furan-containing molecules for pharmaceuticals and agrochemicals. Its boronic acid group facilitates carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and development of bioactive compounds. The ethoxycarbonyl group enhances stability and influences reactivity, allowing selective transformations in heterocyclic chemistry. Commonly employed in the preparation of functionalized furans used in materials science and medicinal chemistry.

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...