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

98%

Reagent Code: #81753
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CAS Number 207857-15-6

science Other reagents with same CAS 207857-15-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 391.36 g/mol
Formula C₁₂H₂₀F₃N₃O₆S
thermostat Physical Properties
Melting Point 113°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized as a versatile reagent in organic synthesis, particularly in the preparation of protected guanidine derivatives. Its trifluoromethylsulfonyl group acts as a strong activating agent, facilitating the introduction of guanidine moieties into various organic molecules. This makes it valuable in the synthesis of pharmaceuticals, where guanidine structures are often key components due to their biological activity. Additionally, the Boc (tert-butoxycarbonyl) protecting groups provide stability and selectivity during multi-step synthetic processes, allowing for controlled reactions and easy deprotection when needed. Its application extends to the development of peptides, peptidomimetics, and other biologically active compounds, where precise functional group manipulation is essential.

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Test Parameter Specification
Purity 98-100%
Melting Point 113

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿8,490.00
inventory 250mg
10-20 days ฿880.00
inventory 1g
10-20 days ฿1,980.00

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1,3-Di-Boc-2-(trifluoromethylsulfonyl)guanidine
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This chemical is primarily utilized as a versatile reagent in organic synthesis, particularly in the preparation of protected guanidine derivatives. Its trifluoromethylsulfonyl group acts as a strong activating agent, facilitating the introduction of guanidine moieties into various organic molecules. This makes it valuable in the synthesis of pharmaceuticals, where guanidine structures are often key components due to their biological activity. Additionally, the Boc (tert-butoxycarbonyl) protecting groups provide stability and selectivity during multi-step synthetic processes, allowing for controlled reactions and easy deprotection when needed. Its application extends to the development of peptides, peptidomimetics, and other biologically active compounds, where precise functional group manipulation is essential.
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