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Structure of 41727-48-4
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Methyl 4-amino-3,5-dichlorobenzoate features a dual functional group architecture: a bench-stable methyl ester paired with a primary amino handle. This combination enables direct incorporation into amide couplings and facilitates downstream derivatization in synthetic routes. The electron-deficient aromatic core enhances reactivity in electrophilic substitution processes.
Methyl 4-amino-3,5-dichlorobenzoate serves as a versatile building block in medicinal chemistry, enabling direct incorporation of the 3,5-dichloroaniline motif into target molecules. The methyl ester group facilitates downstream transformations such as hydrolysis or coupling reactions, while the amino functionality offers reliable site-specific derivatization. Its bench-stable nature and compatibility with standard synthetic protocols make it well-suited for multi-step synthesis of heterocyclic scaffolds 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-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: