4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1,2,3,6-tetrahydropyridine

97%

Reagent Code: #114882
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CAS Number 1256360-46-9

science Other reagents with same CAS 1256360-46-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 363.28 g/mol
Formula C₁₈H₂₆BNO₄S
badge Registry Numbers
MDL Number MFCD17926518
thermostat Physical Properties
Boiling Point 444.2±55.0°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.2±0.1 g/cm3
Storage -20°C, dry sealed

description Product Description

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex molecules. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of heterocyclic compounds, which are essential in drug discovery and medicinal chemistry. The tosyl group enhances stability and reactivity, enabling precise control in multi-step synthetic processes. Its applications extend to material science, where it contributes to the creation of organic electronic components and functional polymers.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿288.00
inventory 250mg
10-20 days ฿423.00
inventory 5g
10-20 days ฿6,219.00
inventory 1g
10-20 days ฿1,530.00

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4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1,2,3,6-tetrahydropyridine
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This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex molecules. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of heterocyclic compounds, which are essential in drug discovery and medicinal chemistry. The tosyl group enh

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex molecules. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of heterocyclic compounds, which are essential in drug discovery and medicinal chemistry. The tosyl group enhances stability and reactivity, enabling precise control in multi-step synthetic processes. Its applications extend to material science, where it contributes to the creation of organic electronic components and functional polymers.

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