(6-chloropyridin-3-yl)(2-methylpiperidin-1-yl)methanone

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Reagent Code: #245776
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CAS Number 385408-28-6

science Other reagents with same CAS 385408-28-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.71 g/mol
Formula C₁₂H₁₅ClN₂O
inventory_2 Storage & Handling
Storage -20°C, Sealed, Dry

description Product Description

Used as a key intermediate in the synthesis of nicotinic acetylcholine receptor modulators, particularly in the development of neonicotinoid insecticides. It contributes to the biological activity and selectivity of crop protection agents by enhancing binding affinity to insect nervous system receptors. Also explored in pharmaceutical research for central nervous system-targeted compounds due to its structural similarity to neuroactive molecules. Its chloropyridin-3-yl and 2-methylpiperidin-1-yl components allow for versatile chemical modifications in agrochemical and medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿28,590.00
inventory 5mg
10-20 days ฿10,990.00
inventory 10mg
10-20 days ฿15,390.00

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(6-chloropyridin-3-yl)(2-methylpiperidin-1-yl)methanone
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Used as a key intermediate in the synthesis of nicotinic acetylcholine receptor modulators, particularly in the development of neonicotinoid insecticides. It contributes to the biological activity and selectivity of crop protection agents by enhancing binding affinity to insect nervous system receptors. Also explored in pharmaceutical research for central nervous system-targeted compounds due to its structural similarity to neuroactive molecules. Its chloropyridin-3-yl and 2-methylpiperidin-1-yl componen

Used as a key intermediate in the synthesis of nicotinic acetylcholine receptor modulators, particularly in the development of neonicotinoid insecticides. It contributes to the biological activity and selectivity of crop protection agents by enhancing binding affinity to insect nervous system receptors. Also explored in pharmaceutical research for central nervous system-targeted compounds due to its structural similarity to neuroactive molecules. Its chloropyridin-3-yl and 2-methylpiperidin-1-yl components allow for versatile chemical modifications in agrochemical and medicinal chemistry.

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