Ethyl 2-(aminomethyl)isonicotinate hydrochloride

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Reagent Code: #182600
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CAS Number 1189983-26-3

science Other reagents with same CAS 1189983-26-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.67 g/mol
Formula C₉H₁₃ClN₂O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) active agents. Its structure supports the formation of bioactive molecules, making it valuable in medicinal chemistry for creating analogs with potential anticonvulsant, anxiolytic, or neuroprotective effects. Commonly employed in research settings to design new drug candidates targeting neurological disorders. Also utilized in the preparation of heterocyclic compounds due to its reactive amine and ester functionalities, enabling a range of derivatization reactions for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿740.00
inventory 250mg
10-20 days ฿2,250.00
inventory 1g
10-20 days ฿6,310.00
inventory 5g
10-20 days ฿28,160.00

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Ethyl 2-(aminomethyl)isonicotinate hydrochloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) active agents. Its structure supports the formation of bioactive molecules, making it valuable in medicinal chemistry for creating analogs with potential anticonvulsant, anxiolytic, or neuroprotective effects. Commonly employed in research settings to design new drug candidates targeting neurological disorders. Also utilized in the preparation of heterocyclic compounds due to it

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) active agents. Its structure supports the formation of bioactive molecules, making it valuable in medicinal chemistry for creating analogs with potential anticonvulsant, anxiolytic, or neuroprotective effects. Commonly employed in research settings to design new drug candidates targeting neurological disorders. Also utilized in the preparation of heterocyclic compounds due to its reactive amine and ester functionalities, enabling a range of derivatization reactions for structure-activity relationship studies.

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