Benzyl 2-(((benzyloxy)carbonyl)amino)-2-(dimethoxyphosphoryl)acetate

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Reagent Code: #41105
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CAS Number 898530-63-7

science Other reagents with same CAS 898530-63-7

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Weight 407.3500 g/mol
Formula C₁₉H₂₂NO₇P
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MDL Number MFCD28396374
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This chemical is primarily used in organic synthesis as a key intermediate in the preparation of phosphonate derivatives, which are valuable in medicinal chemistry and drug development. It plays a role in the synthesis of compounds with potential biological activity, such as enzyme inhibitors or antiviral agents. The presence of both the benzyl and phosphonate groups makes it a versatile building block for constructing complex molecules. Additionally, it can be utilized in peptide chemistry for the protection of amino groups during synthesis, ensuring selective reactions. Its application extends to research laboratories focusing on the development of new pharmaceuticals or bioactive molecules.

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inventory 1g
10-20 days ฿4,572.00

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Benzyl 2-(((benzyloxy)carbonyl)amino)-2-(dimethoxyphosphoryl)acetate
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This chemical is primarily used in organic synthesis as a key intermediate in the preparation of phosphonate derivatives, which are valuable in medicinal chemistry and drug development. It plays a role in the synthesis of compounds with potential biological activity, such as enzyme inhibitors or antiviral agents. The presence of both the benzyl and phosphonate groups makes it a versatile building block for constructing complex molecules. Additionally, it can be utilized in peptide chemistry for the prote

This chemical is primarily used in organic synthesis as a key intermediate in the preparation of phosphonate derivatives, which are valuable in medicinal chemistry and drug development. It plays a role in the synthesis of compounds with potential biological activity, such as enzyme inhibitors or antiviral agents. The presence of both the benzyl and phosphonate groups makes it a versatile building block for constructing complex molecules. Additionally, it can be utilized in peptide chemistry for the protection of amino groups during synthesis, ensuring selective reactions. Its application extends to research laboratories focusing on the development of new pharmaceuticals or bioactive molecules.

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