3-Phenoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

97%

Reagent Code: #225428
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CAS Number 1309981-45-0

science Other reagents with same CAS 1309981-45-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.16 g/mol
Formula C₁₇H₂₀BNO₃
badge Registry Numbers
MDL Number MFCD11617852
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and development of biaryl compounds. Commonly employed in the preparation of pyridine-based active ingredients in crop protection agents and medicinal molecules. Stable and compatible with a wide range of functional groups, it supports high-yield transformations in both research and industrial settings.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿730.00
inventory 250mg
10-20 days ฿1,280.00
inventory 1g
10-20 days ฿4,180.00
inventory 5g
10-20 days ฿17,340.00

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3-Phenoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and development of biaryl compounds. Commonly employed in the preparation of pyridine-based active ingredients in crop protection agents and medicinal molecules. Stable and compatible with a wide range of functional groups, it supports high-yield tran

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and development of biaryl compounds. Commonly employed in the preparation of pyridine-based active ingredients in crop protection agents and medicinal molecules. Stable and compatible with a wide range of functional groups, it supports high-yield transformations in both research and industrial settings.

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