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Structure of 98231-07-3
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Methyl 3,3-dimethoxycyclobutane-1-carboxylate features a cyclobutane core with two methoxy groups at C3, enhancing solubility and stability. This bench-stable ester integrates readily into synthetic sequences requiring strained ring systems, offering predictable reactivity in nucleophilic transformations and serving as a key intermediate in the construction of complex cyclic architectures.
Methyl 3,3-dimethoxycyclobutane-1-carboxylate serves as a versatile building block for cyclobutane-based scaffolds in synthetic organic chemistry. The gem-dimethoxy group enables facile acid-mediated cleavage to generate cyclobutanone intermediates, while the ester functionality supports standard transformations such as reduction, nucleophilic addition, and cross-coupling reactions. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for iterative synthesis workflows in medicinal chemistry and process development.
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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: