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Structure of 163487-10-3
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(E)-Methyl 3-(3-aminophenyl)acrylate features a conjugated acrylate system paired with a para-amino aromatic group, enabling efficient integration into diverse synthetic scaffolds. This electron-rich enone moiety facilitates nucleophilic additions and serves as a key building block in pharmaceutical and agrochemical synthesis. The methyl ester functionality supports further derivatization under standard conditions.
(E)-Methyl 3-(3-aminophenyl)acrylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted anilines and heterocyclic scaffolds. The conjugated enamide system exhibits robust stability under standard bench conditions and tolerates diverse functional groups, facilitating downstream transformations such as Suzuki-Miyaura coupling, electrophilic substitution, and cyclization reactions. Its amine functionality provides a direct handle for derivatization, while the ester group supports selective reduction or hydrolysis—making it particularly valuable in medicinal chemistry lead optimization and API precursor synthesis.
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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: