Atomfair Ethanone, 2-chloro-1-(1-chlorocyclopropyl)- C5H6Cl2O

Description 2-Chloro-1-(1-chlorocyclopropyl)ethanone (CAS No. 120983-72-4) is a highly specialized organic compound with the molecular formula C5H6Cl2O . This chlorinated ketone derivative features a reactive cyclopropyl group, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. With a purity grade suitable for laboratory use, this compound is rigorously tested to ensure consistency and reliability in experimental applications. Its unique structural properties enable its use in the synthesis of complex molecules, including potential agrochemicals and bioactive compounds. Packaged under inert conditions to maintain stability, this product is ideal for researchers requiring high-precision reagents for advanced chemical transformations.

Description

2-Chloro-1-(1-chlorocyclopropyl)ethanone (CAS No. 120983-72-4) is a highly specialized organic compound with the molecular formula C₅H₆Cl₂O. This chlorinated ketone derivative features a reactive cyclopropyl group, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. With a purity grade suitable for laboratory use, this compound is rigorously tested to ensure consistency and reliability in experimental applications. Its unique structural properties enable its use in the synthesis of complex molecules, including potential agrochemicals and bioactive compounds. Packaged under inert conditions to maintain stability, this product is ideal for researchers requiring high-precision reagents for advanced chemical transformations.

CAS No: 120983-72-4
Molecular Formula: C5H6Cl2O
Molecular Weight: 153.00
Exact Mass: 151.9795702
Monoisotopic Mass: 151.9795702
IUPAC Name: 2-chloro-1-(1-chlorocyclopropyl)ethanone
SMILES: C1CC1(C(=O)CCl)Cl
Synonyms: 2-chloro-1-(1-chlorocyclopropyl)ethanone, 120983-72-4, Ethanone, 2-chloro-1-(1-chlorocyclopropyl)-, DTXSID50888254, DTXCID601027534

Application

2-Chloro-1-(1-chlorocyclopropyl)ethanone serves as a versatile building block in organic synthesis, particularly in the development of cyclopropane-containing pharmaceuticals. Researchers utilize this compound in nucleophilic substitution reactions and as a precursor for heterocyclic frameworks. Its reactivity profile makes it suitable for exploring novel pesticidal or herbicidal agents. Additionally, it may be employed in materials science for modifying polymer properties.

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