(S)-5-(1,3-Bis(tert-butoxycarbonyl)guanidino)-2-((tert-butoxycarbonyl)amino)pentanoic acid

≥95%

Reagent Code: #38556
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CAS Number 97745-69-2

science Other reagents with same CAS 97745-69-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 474.55 g/mol
Formula C₂₁H₃₈N₄O₈
badge Registry Numbers
MDL Number MFCD00270489
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a key intermediate in the production of complex peptides, particularly those requiring specific guanidino and amino group protections. The tert-butoxycarbonyl (Boc) groups act as protective moieties, ensuring selective reactivity during peptide chain assembly. It is especially valuable in solid-phase peptide synthesis (SPPS), where controlled deprotection and coupling steps are critical. Additionally, it finds application in the synthesis of peptidomimetics and bioactive peptides, contributing to drug discovery and development processes. Its stability and compatibility with various organic solvents make it a reliable choice for advanced chemical synthesis.

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Test Parameter Specification
Appearance White to yellow powder or crystals
Purity 94.5-100
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,960.00
inventory 250mg
10-20 days ฿7,260.00
inventory 1g
10-20 days ฿24,600.00

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(S)-5-(1,3-Bis(tert-butoxycarbonyl)guanidino)-2-((tert-butoxycarbonyl)amino)pentanoic acid
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This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a key intermediate in the production of complex peptides, particularly those requiring specific guanidino and amino group protections. The tert-butoxycarbonyl (Boc) groups act as protective moieties, ensuring selective reactivity during peptide chain assembly. It is especially valuable in solid-phase peptide synthesis (SPPS), where controlled deprotection and coupling steps are critical. Additionally,

This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a key intermediate in the production of complex peptides, particularly those requiring specific guanidino and amino group protections. The tert-butoxycarbonyl (Boc) groups act as protective moieties, ensuring selective reactivity during peptide chain assembly. It is especially valuable in solid-phase peptide synthesis (SPPS), where controlled deprotection and coupling steps are critical. Additionally, it finds application in the synthesis of peptidomimetics and bioactive peptides, contributing to drug discovery and development processes. Its stability and compatibility with various organic solvents make it a reliable choice for advanced chemical synthesis.

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