rel-(2R,4S)-4-(((benzyloxy)carbonyl)amino)pyrrolidine-2-carboxylic acid

95%

Reagent Code: #51672
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CAS Number 1217611-00-1

science Other reagents with same CAS 1217611-00-1

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Weight 264.2771 g/mol
Formula C₁₃H₁₆N₂O₄
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This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of peptide-based drugs, particularly those targeting protease enzymes. Its structure, featuring both a carboxylic acid group and a protected amine, makes it suitable for constructing complex peptide chains with specific stereochemistry. Additionally, it is employed in the synthesis of biologically active molecules, including inhibitors and modulators of various enzymatic pathways. Its benzyloxycarbonyl (Cbz) protecting group allows for selective deprotection, enabling controlled reactions in multi-step synthetic processes. This compound is also explored in medicinal chemistry for designing novel therapeutic agents with improved efficacy and selectivity.

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inventory 100mg
10-20 days ฿11,910.00

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rel-(2R,4S)-4-(((benzyloxy)carbonyl)amino)pyrrolidine-2-carboxylic acid
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This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of peptide-based drugs, particularly those targeting protease enzymes. Its structure, featuring both a carboxylic acid group and a protected amine, makes it suitable for constructing complex peptide chains with specific stereochemistry. Additionally, it is employed in the synthesis of biologically active molecules, including inhibitors and modulators of var

This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of peptide-based drugs, particularly those targeting protease enzymes. Its structure, featuring both a carboxylic acid group and a protected amine, makes it suitable for constructing complex peptide chains with specific stereochemistry. Additionally, it is employed in the synthesis of biologically active molecules, including inhibitors and modulators of various enzymatic pathways. Its benzyloxycarbonyl (Cbz) protecting group allows for selective deprotection, enabling controlled reactions in multi-step synthetic processes. This compound is also explored in medicinal chemistry for designing novel therapeutic agents with improved efficacy and selectivity.

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