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Structure of 1001336-16-8
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Methyl 4-chloro-2-formylbenzoate features a strategically positioned formyl group flanked by electron-withdrawing chlorine and ester functionalities, enabling direct incorporation into conjugated systems. This ortho-formylated scaffold facilitates efficient coupling reactions and serves as a key intermediate in synthesizing bioactive heterocycles and functional materials under standard conditions.
Methyl 4-chloro-2-formylbenzoate serves as a versatile synthetic intermediate for the construction of biologically relevant heterocycles and functionalized aromatic systems. The ortho-formyl group enables efficient aldol and Mannich reactions, while the ester and chloro substituents provide orthogonal handles for further derivatization. Its bench-stable nature and compatibility with standard coupling and reduction protocols make it well-suited for modular synthesis in medicinal chemistry and process development 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: