3-Allyl-2-chloro-5-methylpyridine

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Reagent Code: #137720
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CAS Number 1203498-97-8

science Other reagents with same CAS 1203498-97-8

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scatter_plot Molecular Information
Weight 167.64 g/mol
Formula C₉H₁₀ClN
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly neonicotinoid insecticides such as imidacloprid. It plays a key role in the production of nicotinic acetylcholine receptor agonists, which target insect nervous systems for pest control. Its pyridine structure enables selective reactivity, making it valuable for constructing complex molecules. Commonly employed in cross-coupling reactions and nucleophilic substitutions to introduce functional groups in active ingredients of plant protection products. Also explored in medicinal chemistry for neuroactive compounds.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿6,540.00
inventory 250mg
10-20 days ฿23,850.00
inventory 1g
10-20 days ฿66,650.00

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3-Allyl-2-chloro-5-methylpyridine
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly neonicotinoid insecticides such as imidacloprid. It plays a key role in the production of nicotinic acetylcholine receptor agonists, which target insect nervous systems for pest control. Its pyridine structure enables selective reactivity, making it valuable for constructing complex molecules. Commonly employed in cross-coupling reactions and nucleophilic substitutions to introduce functional groups in a

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly neonicotinoid insecticides such as imidacloprid. It plays a key role in the production of nicotinic acetylcholine receptor agonists, which target insect nervous systems for pest control. Its pyridine structure enables selective reactivity, making it valuable for constructing complex molecules. Commonly employed in cross-coupling reactions and nucleophilic substitutions to introduce functional groups in active ingredients of plant protection products. Also explored in medicinal chemistry for neuroactive compounds.

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