4,6-DIMETHYLPYRIDINE-3-BORONIC ACID

95%

Reagent Code: #91997
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CAS Number 1001907-68-1

science Other reagents with same CAS 1001907-68-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.97 g/mol
Formula C₇H₁₀BNO₂
thermostat Physical Properties
Boiling Point 316.1±52.0 ℃(Predicted)
inventory_2 Storage & Handling
Density 1.14±0.1g/ml(Predicted)
Storage -20℃, sealed and dry

description Product Description

4,6-dimethylpyridine-3-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, making it a valuable reagent in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl or vinyl halides, facilitating the creation of complex organic molecules. Additionally, it serves as a building block in the development of heterocyclic compounds, which are often key components in drug discovery and material science. The compound’s stability and reactivity make it a preferred choice in catalytic processes and functional group transformations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿82,800.00
inventory 25mg
10-20 days ฿29,700.00
inventory 5mg
10-20 days ฿8,982.00

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4,6-DIMETHYLPYRIDINE-3-BORONIC ACID
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4,6-dimethylpyridine-3-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, making it a valuable reagent in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl or vinyl halides, facilitating the creation of complex organic molecules. Additionally, it serves as a building block in the development of heterocycl

4,6-dimethylpyridine-3-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, making it a valuable reagent in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl or vinyl halides, facilitating the creation of complex organic molecules. Additionally, it serves as a building block in the development of heterocyclic compounds, which are often key components in drug discovery and material science. The compound’s stability and reactivity make it a preferred choice in catalytic processes and functional group transformations.

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