5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(2-((trimethylsilyl)oxy)propan-2-yl)pyridine

98%

Reagent Code: #48202
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CAS Number 1228014-10-5

science Other reagents with same CAS 1228014-10-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 335.32 g/mol
Formula C₁₇H₃₀BNO₃Si
badge Registry Numbers
MDL Number MFCD12198135
inventory_2 Storage & Handling
Density 1.0±0.1 g/cm3
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it acts as a boronic ester reagent. Its structure, featuring a pyridine ring and a boronate ester group, makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical and agrochemical research. The trimethylsilyl-protected hydroxyl group enhances its stability and reactivity, allowing for selective transformations in multi-step syntheses. Additionally, it is employed in the development of advanced materials, including organic semiconductors and ligands for catalytic systems, due to its ability to facilitate precise molecular modifications.

Available Sizes & Pricing

Size Availability Unit Price Quantity
10g
10-20 days ฿37,422.00
250mg
10-20 days ฿3,465.00
5g
10-20 days ฿20,790.00
1g
10-20 days ฿6,921.00
5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(2-((trimethylsilyl)oxy)propan-2-yl)pyridine
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it acts as a boronic ester reagent. Its structure, featuring a pyridine ring and a boronate ester group, makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical and agrochemical research. The trimethylsilyl-protected hydroxyl group enhances its stability and reactivity, allowing for selective transformations in multi-step synth

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it acts as a boronic ester reagent. Its structure, featuring a pyridine ring and a boronate ester group, makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical and agrochemical research. The trimethylsilyl-protected hydroxyl group enhances its stability and reactivity, allowing for selective transformations in multi-step syntheses. Additionally, it is employed in the development of advanced materials, including organic semiconductors and ligands for catalytic systems, due to its ability to facilitate precise molecular modifications.

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