Ethyl 4-chloro-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate

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Reagent Code: #182436
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CAS Number 821791-58-6

science Other reagents with same CAS 821791-58-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.63 g/mol
Formula C₉H₁₀ClNO₃
thermostat Physical Properties
Boiling Point 302.4°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of nicotinic receptor modulators. Its structure supports derivatization for central nervous system-targeted drugs, including those investigated for cognitive disorders and neuropathic pain. Commonly employed in medicinal chemistry for constructing dihydropyridine-based scaffolds with biological activity. Also utilized in agrochemical research for designing novel pesticides with selective mode of action.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,180.00
inventory 1g
10-20 days ฿4,690.00
inventory 5g
10-20 days ฿23,400.00

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Ethyl 4-chloro-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of nicotinic receptor modulators. Its structure supports derivatization for central nervous system-targeted drugs, including those investigated for cognitive disorders and neuropathic pain. Commonly employed in medicinal chemistry for constructing dihydropyridine-based scaffolds with biological activity. Also utilized in agrochemical research for designing novel pesticides with selective mode of action.<

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of nicotinic receptor modulators. Its structure supports derivatization for central nervous system-targeted drugs, including those investigated for cognitive disorders and neuropathic pain. Commonly employed in medicinal chemistry for constructing dihydropyridine-based scaffolds with biological activity. Also utilized in agrochemical research for designing novel pesticides with selective mode of action.

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