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

97%

Reagent Code: #145872
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CAS Number 165963-71-3

science Other reagents with same CAS 165963-71-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 312.2 g/mol
Formula C₁₁H₂₂BrNO₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a protected amine building block in organic synthesis, particularly in pharmaceutical and agrochemical industries. The tert-butyl carbamate (Boc) group provides stability under various reaction conditions while allowing selective deprotection to release the amine when needed. The bromoethoxy linker enables further functionalization through nucleophilic substitution, making this compound valuable in the construction of complex molecules, including drug candidates and bioactive compounds. Its polyether chain enhances solubility in polar solvents, facilitating use in multi-step synthesis and conjugation strategies.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿180.00
100mg
10-20 days ฿550.00
1g
10-20 days ฿2,980.00
5g
10-20 days ฿13,850.00
25g
10-20 days ฿52,500.00
100g
10-20 days ฿168,000.00
250mg
10-20 days ฿960.00
tert-Butyl (2-(2-(2-bromoethoxy)ethoxy)ethyl)carbamate
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Used as a protected amine building block in organic synthesis, particularly in pharmaceutical and agrochemical industries. The tert-butyl carbamate (Boc) group provides stability under various reaction conditions while allowing selective deprotection to release the amine when needed. The bromoethoxy linker enables further functionalization through nucleophilic substitution, making this compound valuable in the construction of complex molecules, including drug candidates and bioactive compounds. Its polye

Used as a protected amine building block in organic synthesis, particularly in pharmaceutical and agrochemical industries. The tert-butyl carbamate (Boc) group provides stability under various reaction conditions while allowing selective deprotection to release the amine when needed. The bromoethoxy linker enables further functionalization through nucleophilic substitution, making this compound valuable in the construction of complex molecules, including drug candidates and bioactive compounds. Its polyether chain enhances solubility in polar solvents, facilitating use in multi-step synthesis and conjugation strategies.

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