Methyl (5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)carbamate

95%

Reagent Code: #209712
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CAS Number 1073372-02-7

science Other reagents with same CAS 1073372-02-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.11 g/mol
Formula C₁₃H₁₉BN₂O₄
badge Registry Numbers
MDL Number MFCD09027078
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a key intermediate in pharmaceutical synthesis, especially in Suzuki-Miyaura cross-coupling reactions. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in constructing complex molecules for drug development. Commonly employed in the preparation of kinase inhibitors and other bioactive compounds containing pyridine scaffolds. The carbamate functionality allows for further derivatization or protection strategies in multi-step synthetic routes. Widely utilized in medicinal chemistry research for lead optimization and library synthesis in the discovery of new therapeutic agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,230.00
inventory 250mg
10-20 days ฿2,260.00
inventory 1g
10-20 days ฿7,040.00

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Methyl (5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)carbamate
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Used primarily as a key intermediate in pharmaceutical synthesis, especially in Suzuki-Miyaura cross-coupling reactions. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in constructing complex molecules for drug development. Commonly employed in the preparation of kinase inhibitors and other bioactive compounds containing pyridine scaffolds. The carbamate functionality allows for further derivatization or protection strategies in multi-step synthetic routes. Wi

Used primarily as a key intermediate in pharmaceutical synthesis, especially in Suzuki-Miyaura cross-coupling reactions. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in constructing complex molecules for drug development. Commonly employed in the preparation of kinase inhibitors and other bioactive compounds containing pyridine scaffolds. The carbamate functionality allows for further derivatization or protection strategies in multi-step synthetic routes. Widely utilized in medicinal chemistry research for lead optimization and library synthesis in the discovery of new therapeutic agents.

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