4-(4-(tert-Butoxycarbonyl)piperazin-1-yl)-4-oxobutanoic acid

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Reagent Code: #46263
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CAS Number 288851-44-5

science Other reagents with same CAS 288851-44-5

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Weight 286.3242 g/mol
Formula C₁₃H₂₂N₂O₅
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MDL Number MFCD06409184
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This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of various biologically active molecules, particularly in the development of drugs targeting neurological and cardiovascular disorders. Its structure, featuring a tert-butoxycarbonyl (Boc) protected piperazine moiety, makes it valuable for peptide synthesis and the creation of complex organic compounds. Additionally, it is employed in the design of protease inhibitors and other therapeutic agents due to its ability to modulate enzyme activity. Its versatility in chemical reactions, such as coupling and deprotection processes, further enhances its utility in medicinal chemistry and drug discovery.

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inventory 1g
10-20 days ฿3,267.00

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4-(4-(tert-Butoxycarbonyl)piperazin-1-yl)-4-oxobutanoic acid
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This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of various biologically active molecules, particularly in the development of drugs targeting neurological and cardiovascular disorders. Its structure, featuring a tert-butoxycarbonyl (Boc) protected piperazine moiety, makes it valuable for peptide synthesis and the creation of complex organic compounds. Additionally, it is employed in the design of protease

This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of various biologically active molecules, particularly in the development of drugs targeting neurological and cardiovascular disorders. Its structure, featuring a tert-butoxycarbonyl (Boc) protected piperazine moiety, makes it valuable for peptide synthesis and the creation of complex organic compounds. Additionally, it is employed in the design of protease inhibitors and other therapeutic agents due to its ability to modulate enzyme activity. Its versatility in chemical reactions, such as coupling and deprotection processes, further enhances its utility in medicinal chemistry and drug discovery.

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