(R)-5-Amino-1-methylpiperidin-2-one

98%

Reagent Code: #229252
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CAS Number 2002478-53-5

science Other reagents with same CAS 2002478-53-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 128.17 g/mol
Formula C₆H₁₂N₂O
badge Registry Numbers
MDL Number MFCD30364322
inventory_2 Storage & Handling
Storage -20°C, light-proof, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules due to the presence of a constrained piperidone ring and an amine group, enabling interactions with biological targets. Commonly employed in the preparation of enzyme inhibitors and receptor modulators where stereochemistry plays a critical role in activity. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid scaffold and functional handles for derivatization.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,900.00
inventory 250mg
10-20 days ฿22,900.00
(R)-5-Amino-1-methylpiperidin-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 agents. Its structure supports the creation of bioactive molecules due to the presence of a constrained piperidone ring and an amine group, enabling interactions with biological targets. Commonly employed in the preparation of enzyme inhibitors and receptor modulators where stereochemistry plays a critical role in activity. Also utilized in medicinal chemistry for structure-activ

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules due to the presence of a constrained piperidone ring and an amine group, enabling interactions with biological targets. Commonly employed in the preparation of enzyme inhibitors and receptor modulators where stereochemistry plays a critical role in activity. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid scaffold and functional handles for derivatization.

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