(R)-2-Amino-6-(((prop-2-yn-1-yloxy)carbonyl)amino)hexanoic acid hydrochloride

95%

Reagent Code: #73160
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CAS Number 1994327-93-3

science Other reagents with same CAS 1994327-93-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.71 g/mol
Formula C₁₀H₁₇ClN₂O₄
badge Registry Numbers
MDL Number MFCD24842519
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of peptide-based therapeutics, particularly those targeting specific enzyme inhibitors or receptor modulators. Its structure, featuring both an amino acid backbone and a propargyloxycarbonyl protecting group, makes it valuable for controlled peptide coupling reactions. Additionally, it is used in the preparation of click chemistry reagents, enabling the conjugation of biomolecules for applications in targeted drug delivery systems and diagnostic probes. Its hydrochloride form ensures stability and solubility, facilitating its use in various biochemical and pharmaceutical processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,982.00
inventory 250mg
10-20 days ฿21,204.00

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(R)-2-Amino-6-(((prop-2-yn-1-yloxy)carbonyl)amino)hexanoic acid hydrochloride
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This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of peptide-based therapeutics, particularly those targeting specific enzyme inhibitors or receptor modulators. Its structure, featuring both an amino acid backbone and a propargyloxycarbonyl protecting group, makes it valuable for controlled peptide coupling reactions. Additionally, it is used in the preparation of click chemistry reagents, enabling the conjugatio

This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of peptide-based therapeutics, particularly those targeting specific enzyme inhibitors or receptor modulators. Its structure, featuring both an amino acid backbone and a propargyloxycarbonyl protecting group, makes it valuable for controlled peptide coupling reactions. Additionally, it is used in the preparation of click chemistry reagents, enabling the conjugation of biomolecules for applications in targeted drug delivery systems and diagnostic probes. Its hydrochloride form ensures stability and solubility, facilitating its use in various biochemical and pharmaceutical processes.

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