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Structure of 2137895-68-0
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Methyl 7-bromo-2,3-dihydrobenzofuran-3-carboxylate features a brominated benzofuran scaffold with a labile ester group, enabling selective functionalization in late-stage synthesis. The electron-deficient aryl ring facilitates transition-metal-catalyzed coupling reactions, while the dihydrofuran core provides conformational rigidity beneficial for medicinal chemistry applications. This compound serves as a key intermediate in the construction of bioactive heterocycles under mild conditions.
Methyl 7-bromo-2,3-dihydrobenzofuran-3-carboxylate serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the bromine site via palladium-catalyzed cross-coupling. The dihydrobenzofuran core provides structural rigidity and favorable pharmacophore geometry, while the ester group permits further derivatization. Bench-stable and compatible with standard reaction conditions, it facilitates efficient access to complex heterocyclic scaffolds relevant to API 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: