1-(4-Methyl-3-pyridinyl)-Ethanone

98%

Reagent Code: #203389
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CAS Number 51227-30-6

science Other reagents with same CAS 51227-30-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 135.167 g/mol
Formula C₈H₉NO
badge Registry Numbers
MDL Number MFCD08447082
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor agonists and antagonists. It serves as a building block in the preparation of compounds with potential applications in treating neurological disorders such as Alzheimer's and Parkinson's disease. Also employed in agrochemical research for the development of novel pesticides due to its structural similarity to nicotinoids. Its pyridinyl core allows for effective binding interactions in biological systems, making it valuable in medicinal chemistry for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,350.00
inventory 1g
10-20 days ฿14,420.00
1-(4-Methyl-3-pyridinyl)-Ethanone
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor agonists and antagonists. It serves as a building block in the preparation of compounds with potential applications in treating neurological disorders such as Alzheimer's and Parkinson's disease. Also employed in agrochemical research for the development of novel pesticides due to its structural similarity to nicotinoids. Its pyridinyl core allows for effective binding interactions in biolog
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor agonists and antagonists. It serves as a building block in the preparation of compounds with potential applications in treating neurological disorders such as Alzheimer's and Parkinson's disease. Also employed in agrochemical research for the development of novel pesticides due to its structural similarity to nicotinoids. Its pyridinyl core allows for effective binding interactions in biological systems, making it valuable in medicinal chemistry for structure-activity relationship studies.
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