(S)-N-(1-aMino-1-oxobutan-2-yl)-4-chlorobutanaMide

>95%

Reagent Code: #71326
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CAS Number 102767-31-7

science Other reagents with same CAS 102767-31-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.08 g/mol
Formula C₈H₁₅ClN₂O₂
badge Registry Numbers
MDL Number MFCD09955129
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its chiral structure makes it valuable for the development of enantiomerically pure drugs, particularly those targeting specific biological pathways. It is often employed in the preparation of protease inhibitors, which are crucial in treating diseases like HIV and hepatitis C. Additionally, its functional groups allow for further chemical modifications, enabling the creation of diverse bioactive molecules with potential therapeutic applications. Researchers also explore its use in peptide mimetics, where it helps mimic the structure and function of natural peptides, aiding in drug discovery and development.

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Test Parameter Specification
Appearance white solid
Purity 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿9,980.00
inventory 250mg
10-20 days ฿25,000.00
inventory 1g
10-20 days ฿56,000.00

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(S)-N-(1-aMino-1-oxobutan-2-yl)-4-chlorobutanaMide
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its chiral structure makes it valuable for the development of enantiomerically pure drugs, particularly those targeting specific biological pathways. It is often employed in the preparation of protease inhibitors, which are crucial in treating diseases like HIV and hepatitis C. Additionally, its functional groups allow for further chemical modifications, enablin

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its chiral structure makes it valuable for the development of enantiomerically pure drugs, particularly those targeting specific biological pathways. It is often employed in the preparation of protease inhibitors, which are crucial in treating diseases like HIV and hepatitis C. Additionally, its functional groups allow for further chemical modifications, enabling the creation of diverse bioactive molecules with potential therapeutic applications. Researchers also explore its use in peptide mimetics, where it helps mimic the structure and function of natural peptides, aiding in drug discovery and development.

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