Methyl 4-[1-(Boc-amino)ethyl]benzoate

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Reagent Code: #46068
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CAS Number 1211572-02-9

science Other reagents with same CAS 1211572-02-9

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Weight 279.3315 g/mol
Formula C₁₅H₂₁NO₄
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MDL Number MFCD24532698
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This chemical is primarily used in organic synthesis as a building block for the preparation of more complex molecules, particularly in pharmaceutical research. It serves as an intermediate in the synthesis of peptides and other bioactive compounds, where the Boc (tert-butoxycarbonyl) group acts as a protective group for amines during reactions. Its structure allows for selective deprotection and further functionalization, making it valuable in the development of drugs and therapeutic agents. Additionally, it is utilized in the study of enzyme inhibitors and receptor ligands due to its ability to mimic natural substrates. Its ester group also enables its use in esterification and transesterification reactions, expanding its versatility in chemical synthesis.

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inventory 100mg
10-20 days ฿9,621.00

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Methyl 4-[1-(Boc-amino)ethyl]benzoate
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This chemical is primarily used in organic synthesis as a building block for the preparation of more complex molecules, particularly in pharmaceutical research. It serves as an intermediate in the synthesis of peptides and other bioactive compounds, where the Boc (tert-butoxycarbonyl) group acts as a protective group for amines during reactions. Its structure allows for selective deprotection and further functionalization, making it valuable in the development of drugs and therapeutic agents. Additionall

This chemical is primarily used in organic synthesis as a building block for the preparation of more complex molecules, particularly in pharmaceutical research. It serves as an intermediate in the synthesis of peptides and other bioactive compounds, where the Boc (tert-butoxycarbonyl) group acts as a protective group for amines during reactions. Its structure allows for selective deprotection and further functionalization, making it valuable in the development of drugs and therapeutic agents. Additionally, it is utilized in the study of enzyme inhibitors and receptor ligands due to its ability to mimic natural substrates. Its ester group also enables its use in esterification and transesterification reactions, expanding its versatility in chemical synthesis.

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