2-(Methylamino)pyridine-4-boronicacidpinacolester

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Reagent Code: #213471
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CAS Number 1350913-08-4

science Other reagents with same CAS 1350913-08-4

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scatter_plot Molecular Information
Weight 234.1 g/mol
Formula C₁₂H₁₉BN₂O₂
badge Registry Numbers
MDL Number MFCD11878218
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active compounds, particularly in pharmaceutical and agrochemical research. Its boronic ester functionality enables efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of kinase inhibitors and other nitrogen-containing heterocyclic drug candidates. Also utilized in materials science for constructing conjugated systems in organic electronics due to its stable pyridine core and reactive handle for further functionalization.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,440.00
inventory 250mg
10-20 days ฿11,030.00
inventory 1g
10-20 days ฿30,860.00

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2-(Methylamino)pyridine-4-boronicacidpinacolester
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active compounds, particularly in pharmaceutical and agrochemical research. Its boronic ester functionality enables efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of kinase inhibitors and other nitrogen-containing heterocyclic drug candidates. Also utilized in materials science for constructing conjugated systems in organic electronics due to its stab

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active compounds, particularly in pharmaceutical and agrochemical research. Its boronic ester functionality enables efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of kinase inhibitors and other nitrogen-containing heterocyclic drug candidates. Also utilized in materials science for constructing conjugated systems in organic electronics due to its stable pyridine core and reactive handle for further functionalization.

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