(R)-Piperidine-3-Carboxylic Acid Ethyl Ester Hydrochloride

≥98%

Reagent Code: #230264
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CAS Number 37675-19-7

science Other reagents with same CAS 37675-19-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.67 g/mol
Formula C₈H₁₆ClNO₂
thermostat Physical Properties
Boiling Point 254ºC
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and nicotinic receptor modulators. Its enantiomerically pure structure makes it valuable for creating biologically active molecules with high specificity. Commonly employed in medicinal chemistry for constructing intermediates in drug discovery programs, especially for treatments targeting neurological disorders. The ester functionality allows for easy modification, enabling further chemical transformations in multistep syntheses.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿790.00
inventory 25g
10-20 days ฿3,280.00

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(R)-Piperidine-3-Carboxylic Acid Ethyl Ester Hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and nicotinic receptor modulators. Its enantiomerically pure structure makes it valuable for creating biologically active molecules with high specificity. Commonly employed in medicinal chemistry for constructing intermediates in drug discovery programs, especially for treatments targeting neurological disorders. The ester functionality allows for easy modification, enabli

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and nicotinic receptor modulators. Its enantiomerically pure structure makes it valuable for creating biologically active molecules with high specificity. Commonly employed in medicinal chemistry for constructing intermediates in drug discovery programs, especially for treatments targeting neurological disorders. The ester functionality allows for easy modification, enabling further chemical transformations in multistep syntheses.

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