Tert-Butyl 2-Acetamidoethylcarbamate

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Reagent Code: #243145
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CAS Number 207129-09-7

science Other reagents with same CAS 207129-09-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.25 g/mol
Formula C₉H₁₈N₂O₃
badge Registry Numbers
MDL Number MFCD09788625
inventory_2 Storage & Handling
Density 1.035±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Tert-Butyl 2-acetamidoethylcarbamate is a protected derivative of ethylenediamine, featuring a tert-butoxycarbonyl (Boc) group on one nitrogen and an acetamido group on the other. It serves as a versatile building block in organic synthesis, particularly for pharmaceutical intermediates and fine chemicals. The dual protection enables selective deprotection, coupling, and functionalization in multi-step reactions, improving stability and solubility. It is commonly used in the preparation of peptidomimetics, beta-amino esters, ethylene diamine derivatives, and active pharmaceutical ingredients (APIs) where precise control over reactivity is essential.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,590.00
inventory 5g
10-20 days ฿5,560.00
inventory 25g
10-20 days ฿19,450.00

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Tert-Butyl 2-Acetamidoethylcarbamate
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Tert-Butyl 2-acetamidoethylcarbamate is a protected derivative of ethylenediamine, featuring a tert-butoxycarbonyl (Boc) group on one nitrogen and an acetamido group on the other. It serves as a versatile building block in organic synthesis, particularly for pharmaceutical intermediates and fine chemicals. The dual protection enables selective deprotection, coupling, and functionalization in multi-step reactions, improving stability and solubility. It is commonly used in the preparation of peptidomimetics,
Tert-Butyl 2-acetamidoethylcarbamate is a protected derivative of ethylenediamine, featuring a tert-butoxycarbonyl (Boc) group on one nitrogen and an acetamido group on the other. It serves as a versatile building block in organic synthesis, particularly for pharmaceutical intermediates and fine chemicals. The dual protection enables selective deprotection, coupling, and functionalization in multi-step reactions, improving stability and solubility. It is commonly used in the preparation of peptidomimetics, beta-amino esters, ethylene diamine derivatives, and active pharmaceutical ingredients (APIs) where precise control over reactivity is essential.
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