N-[2-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]furan-2-carboxamide

95%

Reagent Code: #218383
fingerprint
CAS Number 2246827-33-6

science Other reagents with same CAS 2246827-33-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 343.18198 g/mol
Formula C₁₈H₂₂BNO₅
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical research. The presence of the boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of bioactive compounds and functional materials. Its amide linkage also allows for further derivatization, enhancing its utility in medicinal chemistry for constructing heterocyclic frameworks.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿23,680.00
inventory 1g
10-20 days ฿48,000.00
N-[2-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]furan-2-carboxamide
No image available

Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical research. The presence of the boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of bioactive compounds and functional materials. Its amide linkage also allows for further derivatization, enhancing its utility in medicinal chemistry for

Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical research. The presence of the boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of bioactive compounds and functional materials. Its amide linkage also allows for further derivatization, enhancing its utility in medicinal chemistry for constructing heterocyclic frameworks.

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...