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Structure of 910565-30-9
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Methyl 2-(tetrahydrofuran-3-yl)acetate features a chiral tetrahydrofuran ring that imparts stereochemical control in asymmetric synthesis. This bench-stable ester integrates readily into cascade reactions and serves as a key building block for bioactive molecule construction.
Methyl 2-(tetrahydrofuran-3-yl)acetate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to chiral intermediates through standard functional group manipulations. The tetrahydrofuran ring provides stereochemical control and enhanced solubility, while the ester functionality facilitates nucleophilic acyl substitution, reduction, or coupling reactions. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: