tert-Butyl (3-((3-aminopropyl)(tert-butoxycarbonyl)amino)propyl)(4-((tert-butoxycarbonyl)(3-((tert-butoxycarbonyl)amino)propyl)amino)butyl)carbamate

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Reagent Code: #36620
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CAS Number 128550-06-1

science Other reagents with same CAS 128550-06-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 659.90 g/mol
Formula C₃₃H₆₅N₅O₈
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This specialty chemical is a complex, multi-Boc-protected carbamate derivative featuring branched propyl and butyl chains with multiple tert-butoxycarbonyl (Boc) groups and one free primary amine. It serves as a key intermediate in organic synthesis, particularly for constructing polyamine-based structures in pharmaceutical research, gene delivery systems, dendrimers, and bioactive conjugates. The Boc protecting groups enable selective deprotection and stepwise functionalization, providing precise control over reactivity in multi-step reactions while preventing side reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿33,696.00

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tert-Butyl (3-((3-aminopropyl)(tert-butoxycarbonyl)amino)propyl)(4-((tert-butoxycarbonyl)(3-((tert-butoxycarbonyl)amino)propyl)amino)butyl)carbamate
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This specialty chemical is a complex, multi-Boc-protected carbamate derivative featuring branched propyl and butyl chains with multiple tert-butoxycarbonyl (Boc) groups and one free primary amine. It serves as a key intermediate in organic synthesis, particularly for constructing polyamine-based structures in pharmaceutical research, gene delivery systems, dendrimers, and bioactive conjugates. The Boc protecting groups enable selective deprotection and stepwise functionalization, providing precise contro

This specialty chemical is a complex, multi-Boc-protected carbamate derivative featuring branched propyl and butyl chains with multiple tert-butoxycarbonyl (Boc) groups and one free primary amine. It serves as a key intermediate in organic synthesis, particularly for constructing polyamine-based structures in pharmaceutical research, gene delivery systems, dendrimers, and bioactive conjugates. The Boc protecting groups enable selective deprotection and stepwise functionalization, providing precise control over reactivity in multi-step reactions while preventing side reactions.

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