(S)-Ethyl piperidine-3-carboxylate

98%

Reagent Code: #234255
label
Alias (S)-(+)-piperidine-3-carboxylic acid ethyl ester
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CAS Number 37675-18-6

science Other reagents with same CAS 37675-18-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 157.21 g/mol
Formula C₈H₁₅NO₂
badge Registry Numbers
MDL Number MFCD00792499
thermostat Physical Properties
Boiling Point 102-104 °C/7 mmHg(lit.)
inventory_2 Storage & Handling
Density 1.02 g/cm3
Storage 2~8°C

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotine receptor modulators and drugs targeting neurological disorders such as depression, anxiety, and cognitive dysfunction. Its stereochemistry makes it valuable in developing enantiomerically pure active ingredients. Commonly employed in the preparation of potent nicotinic acetylcholine receptor (nAChR) agonists and antagonists. Also utilized in the development of medicinal chemistry building blocks for structure-activity relationship (SAR) studies due to its rigid piperidine scaffold and functional handle for further derivatization.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿174.00
inventory 1g
10-20 days ฿420.00
inventory 5g
10-20 days ฿660.00
inventory 25g
10-20 days ฿2,390.00
inventory 100g
10-20 days ฿9,490.00
inventory 500g
10-20 days ฿46,670.00

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(S)-Ethyl piperidine-3-carboxylate
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotine receptor modulators and drugs targeting neurological disorders such as depression, anxiety, and cognitive dysfunction. Its stereochemistry makes it valuable in developing enantiomerically pure active ingredients. Commonly employed in the preparation of potent nicotinic acetylcholine receptor (nAChR) agonists and antagonists. Also utilized in the development of medicinal chemistry building blo

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotine receptor modulators and drugs targeting neurological disorders such as depression, anxiety, and cognitive dysfunction. Its stereochemistry makes it valuable in developing enantiomerically pure active ingredients. Commonly employed in the preparation of potent nicotinic acetylcholine receptor (nAChR) agonists and antagonists. Also utilized in the development of medicinal chemistry building blocks for structure-activity relationship (SAR) studies due to its rigid piperidine scaffold and functional handle for further derivatization.

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