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Structure of 31420-52-7
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This monomethyl ester of cis-cyclobutane-1,2-dicarboxylic acid features a rigid, strained cyclobutane core that imparts distinct stereochemical control in synthetic transformations. The ester group enhances solubility in organic solvents while preserving the molecule’s conformational integrity, enabling reliable use in asymmetric synthesis and cycloaddition reactions.
cis-Cyclobutane-1,2-dicarboxylic acid monomethyl ester serves as a valuable chiral building block in synthetic organic chemistry, enabling access to constrained cyclic architectures through standard functional group manipulations. Its defined stereochemistry and bench-stable ester functionality facilitate selective derivatization, including hydrolysis, coupling reactions, and cyclization protocols. The molecule functions effectively in the synthesis of heterocyclic scaffolds and bioactive analogs where rigid cyclobutane motifs are required for conformational control.
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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: