Ethyl N-Boc-oxamidate

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Reagent Code: #58936
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CAS Number 216959-34-1

science Other reagents with same CAS 216959-34-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.22 g/mol
Formula C₉H₁₅NO₅
badge Registry Numbers
MDL Number MFCD01631201
thermostat Physical Properties
Melting Point 115-120 °C
inventory_2 Storage & Handling
Density 1.142 g/cm3
Storage -20°C

description Product Description

Ethyl N-Boc-oxamidate is primarily used in organic synthesis as a protecting group for amines. It is particularly valuable in peptide chemistry, where it helps safeguard amino groups during complex reactions, ensuring selective modification of other functional groups. This compound is also employed in the preparation of intermediates for pharmaceuticals, enabling the synthesis of complex molecules with high precision. Additionally, it finds use in the development of bioactive compounds, where its stability and ease of removal make it a preferred choice for protecting sensitive amine functionalities.

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inventory 1g
10-20 days ฿3,492.00

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Ethyl N-Boc-oxamidate
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Ethyl N-Boc-oxamidate is primarily used in organic synthesis as a protecting group for amines. It is particularly valuable in peptide chemistry, where it helps safeguard amino groups during complex reactions, ensuring selective modification of other functional groups. This compound is also employed in the preparation of intermediates for pharmaceuticals, enabling the synthesis of complex molecules with high precision. Additionally, it finds use in the development of bioactive compounds, where its stabili

Ethyl N-Boc-oxamidate is primarily used in organic synthesis as a protecting group for amines. It is particularly valuable in peptide chemistry, where it helps safeguard amino groups during complex reactions, ensuring selective modification of other functional groups. This compound is also employed in the preparation of intermediates for pharmaceuticals, enabling the synthesis of complex molecules with high precision. Additionally, it finds use in the development of bioactive compounds, where its stability and ease of removal make it a preferred choice for protecting sensitive amine functionalities.

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