1,3-Di-Boc-2-(carboxymethyl)guanidine

98%

Reagent Code: #179991
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CAS Number 158478-76-3

science Other reagents with same CAS 158478-76-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 317.34 g/mol
Formula C₁₃H₂₃N₃O₆
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in peptide synthesis and bioconjugation chemistry, particularly for the selective protection and modification of guanidine groups in arginine residues. Its dual Boc-protected structure allows controlled deprotection steps, enabling sequential coupling reactions in solid-phase peptide synthesis. The carboxymethyl group provides a handle for further functionalization, such as amide bond formation or linker attachment in the development of pharmaceuticals, enzyme inhibitors, or diagnostic probes. Due to its stability and solubility in common organic solvents, it is favored in multi-step syntheses requiring high purity and minimal side reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿25,030.00

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1,3-Di-Boc-2-(carboxymethyl)guanidine
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Used as a key intermediate in peptide synthesis and bioconjugation chemistry, particularly for the selective protection and modification of guanidine groups in arginine residues. Its dual Boc-protected structure allows controlled deprotection steps, enabling sequential coupling reactions in solid-phase peptide synthesis. The carboxymethyl group provides a handle for further functionalization, such as amide bond formation or linker attachment in the development of pharmaceuticals, enzyme inhibitors, or di

Used as a key intermediate in peptide synthesis and bioconjugation chemistry, particularly for the selective protection and modification of guanidine groups in arginine residues. Its dual Boc-protected structure allows controlled deprotection steps, enabling sequential coupling reactions in solid-phase peptide synthesis. The carboxymethyl group provides a handle for further functionalization, such as amide bond formation or linker attachment in the development of pharmaceuticals, enzyme inhibitors, or diagnostic probes. Due to its stability and solubility in common organic solvents, it is favored in multi-step syntheses requiring high purity and minimal side reactions.

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