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*For research and further manufacturing use only, not for direct human use.
Structure of 141743-16-0
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Fmoc-N-(tert-butyloxycarbonylmethyl)glycine features a dual-protecting group architecture, combining the Fmoc moiety for N-terminal protection with a tert-butyl ester for side-chain modulation. This bifunctional design enables selective coupling in peptide synthesis while maintaining stability under standard deprotection conditions.
Fmoc-N-(tert-butyloxycarbonylmethyl)glycine serves as a versatile di-functional building block in peptide synthesis, enabling the incorporation of both Fmoc-protected amines and acid-labile Boc-type side chains. Its structure facilitates orthogonal protection strategies in multi-step syntheses, particularly for peptides requiring selective deprotection sequences. The molecule exhibits good bench stability and simplifies purification due to its solubility profile and well-defined cleavage behavior under standard acidic conditions.
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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 : H302-H315-H319-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: