Ethyl 3-oxopiperidine-2-carboxylate hydrochloride

95%

Reagent Code: #183702
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CAS Number 1253789-62-6

science Other reagents with same CAS 1253789-62-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.66 g/mol
Formula C₈H₁₄ClNO₃
badge Registry Numbers
MDL Number MFCD09261401
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting drugs. Its structure supports the formation of piperidine-based bioactive molecules, commonly found in neuroactive compounds. Frequently employed in the preparation of selective enzyme inhibitors and receptor modulators due to the reactivity of the ketone and ester functional groups. Also utilized in the production of agrochemicals and specialty heterocyclic compounds. The hydrochloride salt form enhances stability and solubility, making it suitable for multi-step synthetic routes in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,670.00
inventory 250mg
10-20 days ฿9,790.00
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Ethyl 3-oxopiperidine-2-carboxylate hydrochloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting drugs. Its structure supports the formation of piperidine-based bioactive molecules, commonly found in neuroactive compounds. Frequently employed in the preparation of selective enzyme inhibitors and receptor modulators due to the reactivity of the ketone and ester functional groups. Also utilized in the production of agrochemicals and specialty heterocyclic compounds. The hydrochloride sal

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting drugs. Its structure supports the formation of piperidine-based bioactive molecules, commonly found in neuroactive compounds. Frequently employed in the preparation of selective enzyme inhibitors and receptor modulators due to the reactivity of the ketone and ester functional groups. Also utilized in the production of agrochemicals and specialty heterocyclic compounds. The hydrochloride salt form enhances stability and solubility, making it suitable for multi-step synthetic routes in medicinal chemistry.

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