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Structure of 63485-50-7
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cis-Methyl 3-hydroxycyclobutanecarboxylate features a stereodefined hydroxyl group and ester functionality within a strained cyclobutane ring. This bench-stable scaffold enables direct incorporation into complex molecular architectures, particularly in the synthesis of bioactive cyclic motifs and natural product analogs.
cis-Methyl 3-hydroxycyclobutanecarboxylate serves as a versatile chiral building block in synthetic organic chemistry, enabling stereoselective functionalization at the C3 position. Its cyclobutane core provides conformational rigidity beneficial for medicinal chemistry applications, while the hydroxyl and ester groups offer orthogonal handles for derivatization. The compound exhibits good bench stability and facilitates efficient transformations in standard coupling, protection, and cyclization protocols.
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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: