CAS 79323-24-3
:2-chloro-3-(chloromethyl)thiophene
Description:
2-Chloro-3-(chloromethyl)thiophene is a heterocyclic organic compound characterized by the presence of a thiophene ring, which is a five-membered aromatic ring containing sulfur. This compound features two chlorine substituents: one at the second position and another chloromethyl group at the third position of the thiophene ring. The presence of these halogen substituents can significantly influence the compound's reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. The chloromethyl group can serve as a reactive site for further functionalization, enhancing its utility in synthetic organic chemistry. Additionally, the compound may exhibit interesting electronic properties due to the electron-withdrawing nature of the chlorine atoms, which can affect its behavior in different chemical environments. As with many chlorinated compounds, it is essential to handle 2-chloro-3-(chloromethyl)thiophene with care due to potential toxicity and environmental concerns associated with chlorinated organic substances.
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Found 4 products.
Morpholin-2-ol hydrochloride
CAS:Formula:C4H10ClNO2Purity:95%Color and Shape:SolidMolecular weight:139.5807Morpholin-2-ol hydrochloride
CAS:Formula:C4H10ClNO2Purity:95%Color and Shape:Solid, PowderMolecular weight:139.58Morpholin-2-ol hydrochloride
CAS:<p>Morpholin-2-ol hydrochloride is a single enantiomer of the racemic drug, loxoprofen. It has been shown to have optical activity, with a specific rotation of +12°. The optical purity of the compound is 98%. Morpholin-2-ol hydrochloride is also an activated form of loxoprofen, which may be due to its ability to undergo nucleophilic substitution reactions. This drug has mutagenic activities and can induce modifications in bacterial DNA. It also inhibits the growth of Chinese hamster cells in vitro and induces mutations in vivo in rats.</p>Purity:Min. 95%



