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Structure of 860344-26-9
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Methyl 4-(2-aminoacetyl)benzoate hydrochloride features a strategically positioned aminoacetyl group that enhances solubility and reactivity in peptide coupling workflows. This bench-stable derivative integrates readily into synthetic sequences requiring polar, nitrogen-rich intermediates. The hydrochloride salt form ensures improved handling and storage stability.
Methyl 4-(2-aminoacetyl)benzoate hydrochloride serves as a versatile building block in medicinal chemistry, enabling direct access to substituted benzamide scaffolds. The aminoacetyl group facilitates efficient derivatization via acylation, alkylation, or cyclization reactions, while the methyl ester offers compatibility with standard reduction and amidation protocols. Bench-stable and readily purified by recrystallization, it functions reliably in multi-step syntheses of bioactive heterocycles and API intermediates.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: