(/-)-N-Alpha-Boc-Amino-Epsilon-Caprolactam

≥97%

Reagent Code: #217542
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CAS Number 179686-45-4

science Other reagents with same CAS 179686-45-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.29 g/mol
Formula C₁₁H₂₀N₂O₃
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a chiral building block in the synthesis of peptidomimetics and bioactive molecules. Its protected amine and lactam ring structure make it ideal for selective ring-opening reactions, enabling the construction of unnatural amino acids and cyclic peptides. Commonly employed in pharmaceutical research to develop enzyme inhibitors and receptor modulators, especially where stereochemistry plays a critical role in activity. The Boc group allows for easy deprotection under mild acidic conditions, facilitating stepwise peptide elongation in solid-phase and solution-phase synthesis. Also utilized in the preparation of macrocyclic compounds and as an intermediate in the development of protease inhibitors and antimicrobial agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,440.00
inventory 250mg
10-20 days ฿1,770.00
inventory 1g
10-20 days ฿4,450.00
inventory 5g
10-20 days ฿13,200.00
inventory 10g
10-20 days ฿26,390.00

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(/-)-N-Alpha-Boc-Amino-Epsilon-Caprolactam
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Used as a chiral building block in the synthesis of peptidomimetics and bioactive molecules. Its protected amine and lactam ring structure make it ideal for selective ring-opening reactions, enabling the construction of unnatural amino acids and cyclic peptides. Commonly employed in pharmaceutical research to develop enzyme inhibitors and receptor modulators, especially where stereochemistry plays a critical role in activity. The Boc group allows for easy deprotection under mild acidic conditions, facili

Used as a chiral building block in the synthesis of peptidomimetics and bioactive molecules. Its protected amine and lactam ring structure make it ideal for selective ring-opening reactions, enabling the construction of unnatural amino acids and cyclic peptides. Commonly employed in pharmaceutical research to develop enzyme inhibitors and receptor modulators, especially where stereochemistry plays a critical role in activity. The Boc group allows for easy deprotection under mild acidic conditions, facilitating stepwise peptide elongation in solid-phase and solution-phase synthesis. Also utilized in the preparation of macrocyclic compounds and as an intermediate in the development of protease inhibitors and antimicrobial agents.

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