CAS 50427-65-1
:Propanoic acid, 2-formyl-3-oxo-, methyl ester
Description:
Propanoic acid, 2-formyl-3-oxo-, methyl ester, also known by its CAS number 50427-65-1, is an organic compound characterized by its ester functional group and a propanoic acid backbone. This compound features a formyl group (-CHO) and a keto group (C=O) at specific positions on the carbon chain, contributing to its reactivity and potential applications in organic synthesis. It is typically a colorless to pale yellow liquid with a distinctive odor, and it is soluble in organic solvents. The presence of both the aldehyde and ketone functionalities allows for various chemical reactions, such as condensation and oxidation, making it useful in the synthesis of more complex molecules. Additionally, this compound may exhibit biological activity, which can be explored for potential applications in pharmaceuticals or agrochemicals. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks if ingested or inhaled.
Formula:C5H6O4
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Found 3 products.
Methyl 2-formyl-3-oxo-propionate
CAS:<p>Methyl 2-formyl-3-oxo-propionate is a reactive chemical that is used to prepare quinolizidines, which are biologically active compounds. It is synthesized from 3-acetylpyridine and formaldehyde in the presence of diborane. The reaction with trifluoroacetic acid leads to the formation of an acid chloride, which can be further reacted with amines to give quinolizidines. This compound has been shown to inhibit adenosine receptor a2a, which may lead to increased blood flow and improved cardiac function.</p>Formula:C5H6O4Purity:Min. 95%Molecular weight:130.1 g/mol
