(S)-4-Hydroxypiperidin-2-one

95%

Reagent Code: #235083
fingerprint
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.

Available Sizes & Pricing

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

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-4-Hydroxypiperidin-2-one
No image available

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.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...