N,N',N''-Tri-boc-guanidine

98%

Reagent Code: #219790
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CAS Number 216584-22-4

science Other reagents with same CAS 216584-22-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 359.42 g/mol
Formula C₁₆H₂₉N₃O₆
badge Registry Numbers
MDL Number MFCD11656061
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a protected guanidine reagent in peptide synthesis and organic chemistry, enabling selective amidine or guanidine group formation without side reactions. Its tri-Boc protection allows for controlled deprotection under mild acidic conditions, making it valuable in multi-step syntheses of pharmaceuticals and bioactive molecules. Commonly employed in the preparation of arginine analogs and enzyme inhibitors where precise functional group manipulation is required. Also utilized in solid-phase synthesis due to its stability and compatibility with various coupling agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿660.00
N,N',N''-Tri-boc-guanidine
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Used as a protected guanidine reagent in peptide synthesis and organic chemistry, enabling selective amidine or guanidine group formation without side reactions. Its tri-Boc protection allows for controlled deprotection under mild acidic conditions, making it valuable in multi-step syntheses of pharmaceuticals and bioactive molecules. Commonly employed in the preparation of arginine analogs and enzyme inhibitors where precise functional group manipulation is required. Also utilized in solid-phase synthes

Used as a protected guanidine reagent in peptide synthesis and organic chemistry, enabling selective amidine or guanidine group formation without side reactions. Its tri-Boc protection allows for controlled deprotection under mild acidic conditions, making it valuable in multi-step syntheses of pharmaceuticals and bioactive molecules. Commonly employed in the preparation of arginine analogs and enzyme inhibitors where precise functional group manipulation is required. Also utilized in solid-phase synthesis due to its stability and compatibility with various coupling agents.

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