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

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Reagent Code: #63032
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CAS Number 1807521-04-5

science Other reagents with same CAS 1807521-04-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.33 g/mol
Formula C₁₂H₂₅NO₄
badge Registry Numbers
MDL Number MFCD28155207
thermostat Physical Properties
Boiling Point 315.5±22.0 °C(Predicted)
inventory_2 Storage & Handling
Density 0.982±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

tert-Butyl 3-(2-(2-(methylamino)ethoxy)ethoxy)propanoate is a specialty chemical intermediate featuring a tert-butyl ester and a diethylene glycol linker with a terminal N-methylamine. It is used in pharmaceutical research for synthesizing complex APIs, linkers in antibody-drug conjugates (ADCs), PROTACs, and prodrugs. The hydrophilic PEG-like chain enhances solubility and drug delivery, while the amine enables conjugation via reductive amination or acylation, and the ester provides selective deprotection under acidic conditions.

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inventory 1g
10-20 days ฿54,747.00

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tert-Butyl 3-(2-(2-(methylamino)ethoxy)ethoxy)propanoate
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tert-Butyl 3-(2-(2-(methylamino)ethoxy)ethoxy)propanoate is a specialty chemical intermediate featuring a tert-butyl ester and a diethylene glycol linker with a terminal N-methylamine. It is used in pharmaceutical research for synthesizing complex APIs, linkers in antibody-drug conjugates (ADCs), PROTACs, and prodrugs. The hydrophilic PEG-like chain enhances solubility and drug delivery, while the amine enables conjugation via reductive amination or acylation, and the ester provides selective deprotectio

tert-Butyl 3-(2-(2-(methylamino)ethoxy)ethoxy)propanoate is a specialty chemical intermediate featuring a tert-butyl ester and a diethylene glycol linker with a terminal N-methylamine. It is used in pharmaceutical research for synthesizing complex APIs, linkers in antibody-drug conjugates (ADCs), PROTACs, and prodrugs. The hydrophilic PEG-like chain enhances solubility and drug delivery, while the amine enables conjugation via reductive amination or acylation, and the ester provides selective deprotection under acidic conditions.

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