CAS 15963-40-3
:Cyclobutanecarboxylic acid, 3-methylene-, methyl ester
Description:
Cyclobutanecarboxylic acid, 3-methylene-, methyl ester, with the CAS number 15963-40-3, is an organic compound characterized by its cyclobutane ring structure, which is a four-membered carbon ring. This compound features a carboxylic acid functional group and a methylene group, contributing to its reactivity and potential applications in organic synthesis. As a methyl ester, it possesses an ester functional group, which typically enhances its solubility in organic solvents and influences its boiling and melting points. The presence of the cyclobutane ring can impart unique strain and reactivity patterns compared to more stable cyclic compounds. This substance may exhibit moderate polarity due to the carboxylic acid and ester functionalities, making it useful in various chemical reactions, including esterification and as a building block in the synthesis of more complex organic molecules. Its specific physical and chemical properties, such as boiling point, melting point, and reactivity, would depend on the molecular interactions and the environment in which it is studied.
Formula:Formula
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Found 4 products.
Cyclobutanecarboxylic acid, 3-methylene-, methyl ester
CAS:Formula:C7H10O2Purity:98%Color and Shape:LiquidMolecular weight:126.1531Methyl 3-methylidenecyclobutane-1-carboxylate
CAS:Methyl 3-methylidenecyclobutane-1-carboxylateFormula:C7H10O2Purity:≥95%Color and Shape: clear. colourless liquidMolecular weight:126.15g/molMethyl 3-methylenecyclobutanecarboxylate
CAS:Formula:C7H10O2Purity:98%Color and Shape:LiquidMolecular weight:126.155Methyl 3-methylenecyclobutanecarboxylate
CAS:Methyl 3-methylenecyclobutanecarboxylate is an organic compound with the chemical formula CH3C(O)CH2CH2COOCH3. It is a colorless liquid that is soluble in organic solvents. Methyl 3-methylenecyclobutanecarboxylate has been studied for its use as a precursor to potassium salts, which are used as catalysts in industrial processes. Methyl 3-methylenecyclobutanecarboxylate has also been identified as a structural factor for the elimination of potassium from cyclopentanone and benzene, factors that contribute to its elimination from the body. This compound can be brominated using potassium tert-butoxide and reactions with other reagents such as lithium chloride or sodium hydroxide to form methyl 3-bromocyclobutanecarboxylate, which can then be dehydrobrominated to form methyl 3-Formula:C7H10O2Purity:Min. 95%Molecular weight:126.15 g/mol
