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Structure of 195877-46-4
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Methyl 2-(cyclopentylamino)acetate hydrochloride features a cyclopentylamino moiety linked to a methyl ester-functionalized acetic acid scaffold, delivering enhanced solubility and stability under standard bench conditions. This bench-stable derivative facilitates efficient incorporation into peptide mimetics and bioactive heterocycles, enabling streamlined synthesis of nitrogen-containing pharmaceutical intermediates.
Methyl 2-(cyclopentylamino)acetate hydrochloride serves as a versatile building block in medicinal chemistry, enabling efficient access to bioactive amine-containing scaffolds. Its stable hydrochloride salt form enhances bench handling and solubility, while the pendant amino group facilitates diverse functionalization via alkylation, acylation, or cyclization reactions. The molecule functions effectively in standard coupling protocols and supports the synthesis of heterocyclic derivatives relevant to pharmaceutical development.
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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: