For research use only. Not for therapeutic Use.
Methyl 3-chloro-3-oxopropionate (Cat NO.: R029176) is a reactive organic intermediate containing ester, ketone, and chloro functional groups. Its structure makes it highly versatile for use in organic synthesis, particularly in the formation of heterocycles, pharmaceuticals, and agrochemicals. The electron-withdrawing chloro and carbonyl groups enhance its reactivity in nucleophilic substitution and condensation reactions. It is often used in the preparation of β-keto esters, enolates, and as a building block in the synthesis of complex molecules requiring functional group diversity and selective transformations.
CAS Number | 37517-81-0 |
Synonyms | (Carbomethoxy)acetyl chloride; (Methoxycarbonyl)acetyl chloride; 2-Methoxycarbonylacetyl chloride; 3-Chloro-3-oxopropanoic acid methyl ester; 3-Methoxy-3-oxopropanoyl chloride; Chlorocarbonylacetic acid methyl ester; Malonic acid chloride monomethyl |
Molecular Formula | C4H5ClO3 |
Purity | ≥95% |
Storage | -20°C |
IUPAC Name | methyl 3-chloro-3-oxopropanoate |
InChI | InChI=1S/C4H5ClO3/c1-8-4(7)2-3(5)6/h2H2,1H3 |
InChIKey | UTBCRHAMJFMIIR-UHFFFAOYSA-N |
SMILES | COC(=O)CC(=O)Cl |
Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |