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Structure of 183742-34-9
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This fluorenylmethoxycarbonyl-protected piperazine derivative features a C-terminal carboxylic acid for conjugation, enabling direct incorporation into peptide chains. The tert-butoxycarbonyl group provides orthogonal protection, while the fluorenylmethoxycarbonyl moiety ensures efficient deprotection under mild basic conditions. Designed for solid-phase synthesis, it delivers high coupling efficiency and minimal side reactions.
This compound serves as a versatile, bench-stable building block for peptide and peptidomimetic synthesis. The fluorenylmethoxy carbonyl (Fmoc) and tert-butoxycarbonyl (Boc) groups enable orthogonal protection in multi-step sequences, while the acetic acid functionality facilitates conjugation via amide bond formation. Its piperazine core provides structural diversity and solubility advantages in synthetic workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: