tert-Butyl 3-(2-(2-bromoethoxy)ethoxy)propanoate

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Reagent Code: #117383
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CAS Number 1381861-91-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.19 g/mol
Formula C₁₁H₂₁BrO₄
badge Registry Numbers
MDL Number MFCD22574821
thermostat Physical Properties
Boiling Point 332.0±22.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical and polymer industries. Its structure, featuring a bromoethoxy group, makes it a valuable intermediate for the preparation of polyethylene glycol (PEG) derivatives, which are widely used in drug delivery systems to enhance solubility and stability of therapeutic compounds. Additionally, it serves as a key building block in the development of functionalized polymers and surfactants, contributing to the creation of materials with tailored properties for specific applications. Its reactivity also allows for use in cross-coupling reactions, enabling the construction of advanced chemical architectures in organic synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days $112.71
inventory 100mg
10-20 days $65.43
inventory 1g
10-20 days $232.10
tert-Butyl 3-(2-(2-bromoethoxy)ethoxy)propanoate
This chemical is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical and polymer industries. Its structure, featuring a bromoethoxy group, makes it a valuable intermediate for the preparation of polyethylene glycol (PEG) derivatives, which are widely used in drug delivery systems to enhance solubility and stability of therapeutic compounds. Additionally, it serves as a key building block in the development of functionalized polymers and surfactants, contributing to the creation of materials with tailored properties for specific applications. Its reactivity also allows for use in cross-coupling reactions, enabling the construction of advanced chemical architectures in organic synthesis.
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