(3S,5S)-3,5-Dimethylpiperazin-2-one

97%

Reagent Code: #236301
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CAS Number 1152112-99-6

science Other reagents with same CAS 1152112-99-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 128.17 g/mol
Formula C₆H₁₂N₂O
badge Registry Numbers
MDL Number MFCD18250093
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its cyclic structure and defined stereochemistry make it valuable in medicinal chemistry for constructing peptidomimetics and enzyme inhibitors. Commonly employed in research settings to design compounds with improved metabolic stability and target selectivity. Also utilized in asymmetric synthesis to introduce specific stereocenters in complex molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,860.00
inventory 250mg
10-20 days ฿12,710.00
inventory 1g
10-20 days ฿37,140.00
inventory 100mg
10-20 days ฿7,620.00
(3S,5S)-3,5-Dimethylpiperazin-2-one
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its cyclic structure and defined stereochemistry make it valuable in medicinal chemistry for constructing peptidomimetics and enzyme inhibitors. Commonly employed in research settings to design compounds with improved metabolic stability and target selectivity. Also utilized in asymmetric synthesis to introduce specific stereoce

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its cyclic structure and defined stereochemistry make it valuable in medicinal chemistry for constructing peptidomimetics and enzyme inhibitors. Commonly employed in research settings to design compounds with improved metabolic stability and target selectivity. Also utilized in asymmetric synthesis to introduce specific stereocenters in complex molecules.

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