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Structure of 628732-09-2
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Methyl 5-bromo-2,3-dihydro-1H-indene-2-carboxylate features a brominated indene core with a pendant methyl ester, enabling direct functionalization at the electron-deficient C5 position. This bench-stable scaffold integrates readily into transition-metal-catalyzed coupling cascades and serves as a key intermediate in synthesizing bioactive heterocycles and pharmaceutical analogs.
Methyl 5-bromo-2,3-dihydro-1H-indene-2-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its stable bromo substituent. The dihydroindene core provides rigidity and spatial control, while the ester functionality allows for further transformations such as hydrolysis or reduction. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for applications in medicinal chemistry and materials science.
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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: