tert-Butyl (2-(2-(2-iodoethoxy)ethoxy)ethyl)carbamate

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Reagent Code: #152930
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CAS Number 1820026-89-8

science Other reagents with same CAS 1820026-89-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 359.2 g/mol
Formula C₁₁H₂₂INO₄
inventory_2 Storage & Handling
Storage 2-8°C, drying away from light

description Product Description

Used as a protected amine building block in organic synthesis, particularly in pharmaceutical and agrochemical research. The tert-butyl carbamate (Boc) group allows for reversible protection of the amine, enabling selective reactions at other functional sites. The triethylene glycol-like iodide tail acts as a linker or spacer, useful in the development of prodrugs, bioconjugates, or polymer-supported compounds. Its iodine terminus can undergo substitution reactions, such as nucleophilic displacement or click chemistry, making it valuable in the design of functional molecules, including drug delivery systems and molecular probes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿930.00
inventory 250mg
10-20 days ฿1,350.00
inventory 1g
10-20 days ฿4,780.00
inventory 5g
10-20 days ฿23,800.00

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tert-Butyl (2-(2-(2-iodoethoxy)ethoxy)ethyl)carbamate
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Used as a protected amine building block in organic synthesis, particularly in pharmaceutical and agrochemical research. The tert-butyl carbamate (Boc) group allows for reversible protection of the amine, enabling selective reactions at other functional sites. The triethylene glycol-like iodide tail acts as a linker or spacer, useful in the development of prodrugs, bioconjugates, or polymer-supported compounds. Its iodine terminus can undergo substitution reactions, such as nucleophilic displacement or c

Used as a protected amine building block in organic synthesis, particularly in pharmaceutical and agrochemical research. The tert-butyl carbamate (Boc) group allows for reversible protection of the amine, enabling selective reactions at other functional sites. The triethylene glycol-like iodide tail acts as a linker or spacer, useful in the development of prodrugs, bioconjugates, or polymer-supported compounds. Its iodine terminus can undergo substitution reactions, such as nucleophilic displacement or click chemistry, making it valuable in the design of functional molecules, including drug delivery systems and molecular probes.

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