3-(Aminomethyl)-6-methyl-4-(methylthio)pyridin-2(1H)-one Hydrochloride

≥95%

Reagent Code: #139179
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CAS Number 2326565-23-3

science Other reagents with same CAS 2326565-23-3

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scatter_plot Molecular Information
Weight 220.72 g/mol
Formula C₈H₁₃ClN₂OS
badge Registry Numbers
MDL Number MFCD32876885
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting neurological disorders. Its structure supports the creation of compounds with dopaminergic activity, making it valuable in research for Parkinson’s disease treatments. Also employed in the preparation of selective enzyme inhibitors due to its ability to interact with specific biological targets. The compound's functional groups allow for easy modification, enabling the design of novel drug candidates in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,530.00

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3-(Aminomethyl)-6-methyl-4-(methylthio)pyridin-2(1H)-one Hydrochloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting neurological disorders. Its structure supports the creation of compounds with dopaminergic activity, making it valuable in research for Parkinson’s disease treatments. Also employed in the preparation of selective enzyme inhibitors due to its ability to interact with specific biological targets. The compound's functional groups allow for easy modification, enabling the design of novel drug c

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting neurological disorders. Its structure supports the creation of compounds with dopaminergic activity, making it valuable in research for Parkinson’s disease treatments. Also employed in the preparation of selective enzyme inhibitors due to its ability to interact with specific biological targets. The compound's functional groups allow for easy modification, enabling the design of novel drug candidates in medicinal chemistry.

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