N-Ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinamide

98%

Reagent Code: #214694
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CAS Number 1006876-28-3

science Other reagents with same CAS 1006876-28-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.13 g/mol
Formula C₁₄H₂₁BN₂O₃
badge Registry Numbers
MDL Number MFCD13191367
thermostat Physical Properties
Melting Point 52-54 °C
Boiling Point 438.9±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.09±0.1 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used in Suzuki-Miyaura cross-coupling reactions as a key boronic ester precursor in the synthesis of pharmaceuticals and agrochemicals. Its amide functionality enhances stability and solubility, making it suitable for late-stage functionalization in drug discovery. Commonly employed in the preparation of kinase inhibitors and other bioactive molecules due to its reliable reactivity and compatibility with diverse reaction conditions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿9,120.00
1g
10-20 days ฿23,680.00
5g
10-20 days ฿82,840.00
N-Ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinamide
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Used in Suzuki-Miyaura cross-coupling reactions as a key boronic ester precursor in the synthesis of pharmaceuticals and agrochemicals. Its amide functionality enhances stability and solubility, making it suitable for late-stage functionalization in drug discovery. Commonly employed in the preparation of kinase inhibitors and other bioactive molecules due to its reliable reactivity and compatibility with diverse reaction conditions.

Used in Suzuki-Miyaura cross-coupling reactions as a key boronic ester precursor in the synthesis of pharmaceuticals and agrochemicals. Its amide functionality enhances stability and solubility, making it suitable for late-stage functionalization in drug discovery. Commonly employed in the preparation of kinase inhibitors and other bioactive molecules due to its reliable reactivity and compatibility with diverse reaction conditions.

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