CAS 20497-95-4
:Propanoic acid, 3-nitro-, methyl ester
Description:
Propanoic acid, 3-nitro-, methyl ester, also known by its CAS number 20497-95-4, is an organic compound characterized by the presence of a propanoic acid backbone with a nitro group at the third carbon and a methyl ester functional group. This compound typically appears as a colorless to pale yellow liquid with a distinctive odor. It is soluble in organic solvents and exhibits moderate solubility in water due to the presence of both hydrophobic and hydrophilic regions in its molecular structure. The nitro group contributes to its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and reductions. Additionally, the methyl ester functionality allows for esterification reactions and can influence the compound's volatility and boiling point. As with many nitro compounds, it may exhibit some degree of toxicity and should be handled with care in laboratory settings. Overall, propanoic acid, 3-nitro-, methyl ester is of interest in synthetic organic chemistry and may have applications in pharmaceuticals or agrochemicals.
Formula:C4H7NO4
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Found 1 products.
Methyl 3-nitropropanoate
CAS:<p>Methyl 3-nitropropanoate is a chemical compound that is used in synthetic organic chemistry. It can be synthesized by the nitration of propionic acid and then reacting the product with methyl iodide. This reaction produces an asymmetric synthesis of an α-lactam ring, which is one of the most commonly found functional groups in natural products. The carbonyl group on this molecule is also reactive to many other reagents, which enables it to be modified for use in various methods. The lactam ring has been shown to have anti-inflammatory properties, focusing research on its potential medicinal uses.</p>Formula:C4H7NO4Purity:Min. 95%Molecular weight:133.1 g/mol
