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Structure of 939768-64-6
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tert-Butyl cis-3-hydroxycyclobutane-1-carboxylate features a strained cyclobutane core with a stereochemically defined hydroxyl group and a bench-stable tert-butyl ester. This configuration enables direct incorporation into complex molecular architectures, where the hydroxyl moiety serves as a handle for selective derivatization. The cis arrangement ensures predictable conformational behavior in synthetic sequences.
tert-Butyl cis-3-hydroxycyclobutane-1-carboxylate serves as a versatile chiral building block in synthetic organic chemistry, enabling stereoselective functionalization at the C3 hydroxyl position. The cyclobutane core provides conformational rigidity beneficial for medicinal chemistry applications, while the tert-butyl ester offers bench stability and facile deprotection under mild acidic conditions. Its well-defined stereochemistry supports predictable reactivity in coupling, oxidation, and cyclization processes relevant to heterocyclic and natural product synthesis.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: