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

≥95%

Reagent Code: #116923
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CAS Number 1083168-94-8

science Other reagents with same CAS 1083168-94-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.09 g/mol
Formula C₁₂H₁₇BN₂O₅
badge Registry Numbers
MDL Number MFCD12923397
thermostat Physical Properties
Boiling Point 387.9±42.0°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, where it serves as a key intermediate. Its boronate ester group makes it valuable in Suzuki-Miyaura coupling reactions, enabling the formation of carbon-carbon bonds with high efficiency. This property is especially useful in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its nitro and methoxy substituents contribute to its reactivity, allowing for further functionalization in complex molecular constructions. The compound is often employed in the synthesis of heterocyclic compounds, which are crucial in drug discovery and material science. Its stability and versatility make it a preferred choice for researchers working on fine chemical synthesis and medicinal chemistry projects.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,436.00
inventory 5g
10-20 days ฿21,582.00
inventory 250mg
10-20 days ฿2,187.00

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2-Methoxy-3-nitro-5-(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, where it serves as a key intermediate. Its boronate ester group makes it valuable in Suzuki-Miyaura coupling reactions, enabling the formation of carbon-carbon bonds with high efficiency. This property is especially useful in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its nitro and methoxy substituents contribute to its reactivity, allowing for further function

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate. Its boronate ester group makes it valuable in Suzuki-Miyaura coupling reactions, enabling the formation of carbon-carbon bonds with high efficiency. This property is especially useful in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its nitro and methoxy substituents contribute to its reactivity, allowing for further functionalization in complex molecular constructions. The compound is often employed in the synthesis of heterocyclic compounds, which are crucial in drug discovery and material science. Its stability and versatility make it a preferred choice for researchers working on fine chemical synthesis and medicinal chemistry projects.

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