CAS 143955-12-8
:Cyclopropanecarboxylic acid, 2-acetyl-, methyl ester (9CI)
Description:
Cyclopropanecarboxylic acid, 2-acetyl-, methyl ester (9CI), with the CAS number 143955-12-8, is an organic compound characterized by its cyclopropane ring structure, which contributes to its unique chemical properties. This compound features a carboxylic acid functional group and an ester group, specifically a methyl ester, which influences its reactivity and solubility. The presence of the acetyl group at the second position of the cyclopropane ring adds to its complexity and can affect its biological activity. Typically, compounds like this may exhibit moderate polarity due to the functional groups, making them soluble in organic solvents while having limited solubility in water. Cyclopropanecarboxylic acid derivatives are often studied for their potential applications in pharmaceuticals and agrochemicals, as well as their roles in synthetic organic chemistry. The unique strain of the cyclopropane ring can lead to interesting reactivity patterns, making it a subject of interest in various chemical research fields.
Formula:C7H10O3
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Found 1 products.
Methyl 2-acetylcyclopropane-1-carboxylate
CAS:Methyl 2-acetylcyclopropane-1-carboxylate is a chiral compound that can be synthesized in an asymmetric synthesis. It has been used as a chiral building block for the synthesis of various amines and esters. The diastereoisomers of methyl 2-acetylcyclopropane-1-carboxylate are enantiomers, which means they are mirror images and cannot be superimposed on each other. The two enantiomers have different chemical and physical properties. Methyl 2-acetylcyclopropane-1-carboxylate also reacts with tryptamine to form N,N'-dimethylindole carboxamide or indole carboxamide, which is a biologically active molecule.Formula:C7H10O3Purity:Min. 95%Molecular weight:142.15 g/mol
