(S)-3-((tert-Butoxycarbonyl)amino)-3-(3-chlorophenyl)propanoic acid

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Reagent Code: #50813
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CAS Number 500770-74-1

science Other reagents with same CAS 500770-74-1

blur_circular Chemical Specifications

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Weight 299.7500 g/mol
Formula C₁₄H₁₈ClNO₄
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MDL Number MFCD03427921
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This compound is primarily used in the field of organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the production of biologically active molecules, especially those targeting neurological and psychiatric disorders. Its structure, featuring a chiral center and a protected amino group, makes it valuable for constructing complex drug candidates with specific stereochemical requirements. Additionally, it is utilized in peptide synthesis and as a building block for creating compounds with potential therapeutic applications in areas such as pain management and inflammation. Its versatility and stability under various reaction conditions make it a preferred choice in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,989.00

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(S)-3-((tert-Butoxycarbonyl)amino)-3-(3-chlorophenyl)propanoic acid
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This compound is primarily used in the field of organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the production of biologically active molecules, especially those targeting neurological and psychiatric disorders. Its structure, featuring a chiral center and a protected amino group, makes it valuable for constructing complex drug candidates with specific stereochemical requirements. Additionally, it is utilized in peptide synthesis and as a building

This compound is primarily used in the field of organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the production of biologically active molecules, especially those targeting neurological and psychiatric disorders. Its structure, featuring a chiral center and a protected amino group, makes it valuable for constructing complex drug candidates with specific stereochemical requirements. Additionally, it is utilized in peptide synthesis and as a building block for creating compounds with potential therapeutic applications in areas such as pain management and inflammation. Its versatility and stability under various reaction conditions make it a preferred choice in medicinal chemistry research.

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