ethyl 6-chloro-5-nitropyridine-3-carboxylate

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Reagent Code: #185443
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CAS Number 171876-22-5

science Other reagents with same CAS 171876-22-5

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inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and other central nervous system agents. Commonly employed in medicinal chemistry for constructing pyridine-based drug candidates due to its reactive chloro and nitro functional groups, which allow further substitution and transformation. Also utilized in agrochemical research for developing novel pesticides and herbicides where pyridine derivatives show biological activity. Its ester group facilitates solubility and reactivity in multi-step organic syntheses.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿970.00
inventory 250mg
10-20 days ฿1,390.00
inventory 1g
10-20 days ฿3,050.00
inventory 5g
10-20 days ฿12,010.00
inventory 25g
10-20 days ฿44,230.00

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ethyl 6-chloro-5-nitropyridine-3-carboxylate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and other central nervous system agents. Commonly employed in medicinal chemistry for constructing pyridine-based drug candidates due to its reactive chloro and nitro functional groups, which allow further substitution and transformation. Also utilized in agrochemical research for developing novel pesticides and herbicides where pyridine derivatives show biological activity. Its e

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and other central nervous system agents. Commonly employed in medicinal chemistry for constructing pyridine-based drug candidates due to its reactive chloro and nitro functional groups, which allow further substitution and transformation. Also utilized in agrochemical research for developing novel pesticides and herbicides where pyridine derivatives show biological activity. Its ester group facilitates solubility and reactivity in multi-step organic syntheses.

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