(2S)-(1-Tetrahydropyramid-2-one)-3-methylbutanoic acid

≥95%

Reagent Code: #36505
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CAS Number 192725-50-1

science Other reagents with same CAS 192725-50-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.23 g/mol
Formula C₉H₁₆N₂O₃
thermostat Physical Properties
Boiling Point 440.8±24.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.176g/cm3
Storage 2-8℃, dry

description Product Description

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of drugs targeting neurological and cardiovascular disorders. Its unique structure allows it to act as a chiral building block, enabling the production of enantiomerically pure compounds, which are crucial for enhancing drug efficacy and reducing side effects. Additionally, it is employed in research laboratories for studying enzyme inhibition and receptor binding activities, contributing to the discovery of novel therapeutic agents. Its application extends to the field of organic chemistry, where it serves as a key reagent in asymmetric synthesis, facilitating the creation of complex molecules with high stereochemical control.

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Test Parameter Specification
Appearance White to Beige Solid
Purity (%) 95-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿10,287.00

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(2S)-(1-Tetrahydropyramid-2-one)-3-methylbutanoic acid
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This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of drugs targeting neurological and cardiovascular disorders. Its unique structure allows it to act as a chiral building block, enabling the production of enantiomerically pure compounds, which are crucial for enhancing drug efficacy and reducing side effects. Additionally, it is employed in research laboratories for studying enzyme inhibition and receptor binding activities, contributing

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of drugs targeting neurological and cardiovascular disorders. Its unique structure allows it to act as a chiral building block, enabling the production of enantiomerically pure compounds, which are crucial for enhancing drug efficacy and reducing side effects. Additionally, it is employed in research laboratories for studying enzyme inhibition and receptor binding activities, contributing to the discovery of novel therapeutic agents. Its application extends to the field of organic chemistry, where it serves as a key reagent in asymmetric synthesis, facilitating the creation of complex molecules with high stereochemical control.

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