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Structure of 147687-15-8
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This fluorenylmethyl carbamate derivative features a protected amine moiety with enhanced solubility and stability under standard conditions. The hydroxyethyl side chain enables efficient coupling in peptide synthesis, while the methyl group reduces aggregation. Designed for robust handling in automated workflows.
(9H-Fluoren-9-yl)methyl (2-hydroxyethyl)(methyl)carbamate serves as a robust, bench-stable carbamate protecting group for primary amines in peptide synthesis and medicinal chemistry. It facilitates efficient Nα-amination via nucleophilic displacement, exhibits excellent functional group tolerance, and enables straightforward deprotection under mild acidic conditions. Its solubility profile and compatibility with standard coupling protocols make it ideal for scalable synthesis and automated platforms.
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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
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: