Methyl 6-(1H-pyrazol-1-yl)nicotinate

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Reagent Code: #120449
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CAS Number 321533-62-4

science Other reagents with same CAS 321533-62-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.20 g/mol
Formula C₁₀H₉N₃O₂
badge Registry Numbers
MDL Number MFCD00140746
thermostat Physical Properties
Boiling Point 330.8°C at 760 mmHg
inventory_2 Storage & Handling
Storage room temperature, stored under inert gas

description Product Description

Methyl 6-(1H-pyrazol-1-yl)nicotinate is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex chemical compounds. Its structure, featuring both a pyrazole and a nicotinate moiety, makes it valuable in the synthesis of pharmaceuticals, particularly in the creation of molecules with potential biological activity. It is often employed in the preparation of compounds that are investigated for their therapeutic properties, such as anti-inflammatory, antimicrobial, or anticancer agents. Additionally, its reactivity allows it to be used in the construction of heterocyclic frameworks, which are common in drug discovery and medicinal chemistry. Researchers also explore its application in the development of agrochemicals, where it serves as a building block for designing novel pesticides or herbicides.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿10,440.00
inventory 1g
10-20 days ฿2,583.00
inventory 100mg
10-20 days ฿693.00
inventory 250mg
10-20 days ฿1,035.00

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Methyl 6-(1H-pyrazol-1-yl)nicotinate
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Methyl 6-(1H-pyrazol-1-yl)nicotinate is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex chemical compounds. Its structure, featuring both a pyrazole and a nicotinate moiety, makes it valuable in the synthesis of pharmaceuticals, particularly in the creation of molecules with potential biological activity. It is often employed in the preparation of compounds that are investigated for their therapeutic properties, such as anti-inflammatory, antimicrobial, or anticancer agents. Additionally, its reactivity allows it to be used in the construction of heterocyclic frameworks, which are common in drug discovery and medicinal chemistry. Researchers also explore its application in the development of agrochemicals, where it serves as a building block for designing novel pesticides or herbicides.
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