(S)-4-Hydroxypiperidin-2-one

95%

Reagent Code: #235083
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CAS Number 476014-92-3

science Other reagents with same CAS 476014-92-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 115.13 g/mol
Formula C₅H₉NO₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its structural motif appears in compounds targeting neurological disorders such as Parkinson’s disease and schizophrenia. The (S)-enantiomer is preferred in certain drug candidates due to its higher biological activity and selectivity. It also serves as an intermediate in the preparation of enzyme inhibitors and receptor modulators, especially those involving GABAergic or dopaminergic pathways. Its hydroxyl and carbonyl functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿2,050.00
inventory 100mg
10-20 days ฿4,910.00
inventory 250mg
10-20 days ฿7,990.00
inventory 1g
10-20 days ฿22,310.00
inventory 5g
10-20 days ฿84,590.00

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(S)-4-Hydroxypiperidin-2-one
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its structural motif appears in compounds targeting neurological disorders such as Parkinson’s disease and schizophrenia. The (S)-enantiomer is preferred in certain drug candidates due to its higher biological activity and selectivity. It also serves as an intermediate in the preparation of enzyme inhibitors and receptor modulators, especially those involving GABAer

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its structural motif appears in compounds targeting neurological disorders such as Parkinson’s disease and schizophrenia. The (S)-enantiomer is preferred in certain drug candidates due to its higher biological activity and selectivity. It also serves as an intermediate in the preparation of enzyme inhibitors and receptor modulators, especially those involving GABAergic or dopaminergic pathways. Its hydroxyl and carbonyl functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for structure-activity relationship (SAR) studies.

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