Boc-β-Homolys(Z)-OH

98%

Reagent Code: #60711
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CAS Number 346694-77-7

science Other reagents with same CAS 346694-77-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 394.46 g/mol
Formula C₂₀H₃₀N₂O₆
badge Registry Numbers
MDL Number MFCD01862937
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Boc-β-Homolys(Z)-OH is a protected derivative of β-homolysine, an unnatural amino acid analog. The α-amino group is protected with a tert-butoxycarbonyl (Boc) group, and the side-chain ε-amino group is protected with a benzyloxycarbonyl (Z or Cbz) group. It serves as a key building block in solid-phase peptide synthesis (SPPS), enabling the incorporation of β-homolysine into peptide sequences. This compound is essential for creating modified peptides and peptidomimetics with enhanced stability or biological properties, particularly in pharmaceutical research, drug development, and studies of protein function.

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Test Parameter Specification
Appearance White to Off-white Solid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,224.00
inventory 1g
10-20 days ฿3,834.00

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Boc-β-Homolys(Z)-OH
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Boc-β-Homolys(Z)-OH is a protected derivative of β-homolysine, an unnatural amino acid analog. The α-amino group is protected with a tert-butoxycarbonyl (Boc) group, and the side-chain ε-amino group is protected with a benzyloxycarbonyl (Z or Cbz) group. It serves as a key building block in solid-phase peptide synthesis (SPPS), enabling the incorporation of β-homolysine into peptide sequences. This compound is essential for creating modified peptides and peptidomimetics with enhanced stability or biologi

Boc-β-Homolys(Z)-OH is a protected derivative of β-homolysine, an unnatural amino acid analog. The α-amino group is protected with a tert-butoxycarbonyl (Boc) group, and the side-chain ε-amino group is protected with a benzyloxycarbonyl (Z or Cbz) group. It serves as a key building block in solid-phase peptide synthesis (SPPS), enabling the incorporation of β-homolysine into peptide sequences. This compound is essential for creating modified peptides and peptidomimetics with enhanced stability or biological properties, particularly in pharmaceutical research, drug development, and studies of protein function.

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