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

98%

Reagent Code: #119485
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CAS Number 758699-74-0

science Other reagents with same CAS 758699-74-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.09 g/mol
Formula C₁₂H₁₈BNO₃
badge Registry Numbers
MDL Number MFCD07367561
thermostat Physical Properties
Boiling Point 346.7°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable for creating carbon-carbon bonds. This compound is often employed in the synthesis of biologically active compounds, including potential drug candidates, due to its stability and reactivity under mild conditions. Additionally, it finds use in material science for designing organic electronic materials and polymers. Its versatility in various synthetic pathways highlights its importance in advancing chemical and medicinal research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿783.00
inventory 50mg
10-20 days ฿630.00
inventory 250mg
10-20 days ฿1,035.00

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4-Methoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable for creating carbon-carbon bonds. This compound is often employed in the synthesis of biologically active compounds, including potential drug candidate

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable for creating carbon-carbon bonds. This compound is often employed in the synthesis of biologically active compounds, including potential drug candidates, due to its stability and reactivity under mild conditions. Additionally, it finds use in material science for designing organic electronic materials and polymers. Its versatility in various synthetic pathways highlights its importance in advancing chemical and medicinal research.

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