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Structure of 36065-27-7
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N-(1-Phenylethyl)acetamide features a chiral benzylic center flanked by an acetamide group, enabling selective functionalization in asymmetric synthesis. This bench-stable compound integrates readily into peptide-like scaffolds and serves as a key intermediate in the development of bioactive molecules requiring defined stereochemistry and controlled solubility.
N-(1-Phenylethyl)acetamide serves as a stable, bench-ready amide building block for the synthesis of chiral intermediates. Its tertiary α-carbon enables stereoselective transformations, while the acetamide group offers compatibility with standard functional group manipulations. The molecule functions effectively in asymmetric synthesis and provides predictable reactivity in coupling and reduction protocols.
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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: