(R)-2-((((Benzyloxy)carbonyl)amino)methyl)-4-methylpentanoic acid

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Reagent Code: #37435
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CAS Number 132606-01-0

science Other reagents with same CAS 132606-01-0

blur_circular Chemical Specifications

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Weight 279.3315 g/mol
Formula C₁₅H₂₁NO₄
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Storage room temperature

description Product Description

This compound is primarily utilized in the synthesis of peptides and peptidomimetics, serving as a key intermediate in the development of biologically active molecules. Its structure, featuring a benzyloxycarbonyl (Cbz) protecting group, makes it valuable in organic chemistry for protecting amine functionalities during multi-step synthesis processes. It is often employed in the preparation of chiral compounds, particularly in pharmaceutical research, where enantiomeric purity is critical for drug efficacy and safety. Additionally, it can be used in the study of enzyme inhibitors and receptor ligands, aiding in the discovery of new therapeutic agents. Its application extends to material science, where it contributes to the design of advanced polymers and biomaterials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,415.00

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(R)-2-((((Benzyloxy)carbonyl)amino)methyl)-4-methylpentanoic acid
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This compound is primarily utilized in the synthesis of peptides and peptidomimetics, serving as a key intermediate in the development of biologically active molecules. Its structure, featuring a benzyloxycarbonyl (Cbz) protecting group, makes it valuable in organic chemistry for protecting amine functionalities during multi-step synthesis processes. It is often employed in the preparation of chiral compounds, particularly in pharmaceutical research, where enantiomeric purity is critical for drug efficac

This compound is primarily utilized in the synthesis of peptides and peptidomimetics, serving as a key intermediate in the development of biologically active molecules. Its structure, featuring a benzyloxycarbonyl (Cbz) protecting group, makes it valuable in organic chemistry for protecting amine functionalities during multi-step synthesis processes. It is often employed in the preparation of chiral compounds, particularly in pharmaceutical research, where enantiomeric purity is critical for drug efficacy and safety. Additionally, it can be used in the study of enzyme inhibitors and receptor ligands, aiding in the discovery of new therapeutic agents. Its application extends to material science, where it contributes to the design of advanced polymers and biomaterials.

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