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Structure of 1350821-95-2
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Methyl 4-(hydroxymethyl)bicyclo[2.2.1]heptane-1-carboxylate features a rigid bicyclic framework with a pendant hydroxymethyl group, offering a stereodefined scaffold for synthetic exploration. The ester functionality enables selective derivatization, while the hydroxymethyl moiety provides a handle for further functionalization under standard conditions. This compound serves as a valuable building block in asymmetric synthesis and medicinal chemistry.
Methyl 4-(hydroxymethyl)bicyclo[2.2.1]heptane-1-carboxylate serves as a versatile synthetic building block for strained bicyclic architectures, enabling efficient access to functionalized norbornane derivatives. The pendant hydroxymethyl group offers direct handle for oxidation, protection, or conjugation, while the ester moiety facilitates selective transformations. Its robust bench stability and compatibility with standard coupling and reduction protocols make it ideal for medicinal chemistry campaigns requiring rigid, three-dimensional scaffolds.
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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: