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Structure of 17841-69-9
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Ethyl 2-(4-(aminomethyl)phenyl)acetate hydrochloride features a pendant primary amine anchored to a phenyl ring, enabling direct functionalization in peptide and bioconjugation workflows. This bench-stable, moisture-tolerant derivative integrates readily into diverse synthetic sequences under standard conditions.
Ethyl 2-(4-(aminomethyl)phenyl)acetate hydrochloride serves as a versatile building block for the synthesis of biologically active arylalkylamine derivatives. The protected amine functionality enables straightforward functionalization, while the ester group supports orthogonal transformations. Its bench-stable solid form and compatibility with standard coupling reactions facilitate efficient access to pharmaceutical intermediates and heterocyclic scaffolds in medicinal chemistry 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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: