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CAS 31581-11-0

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2,3-Bis(chloromethyl)-1,4-naphthoquinone

Description:
2,3-Bis(chloromethyl)-1,4-naphthoquinone is a synthetic organic compound characterized by its naphthoquinone structure, which features two chloromethyl groups at the 2 and 3 positions of the naphthoquinone ring. This compound is typically a yellow to orange solid, exhibiting a range of chemical properties due to the presence of both the naphthoquinone moiety and the chloromethyl substituents. It is known for its reactivity, particularly in electrophilic substitution reactions, and can participate in various chemical transformations, making it useful in organic synthesis. The chloromethyl groups enhance its electrophilic character, allowing it to engage in nucleophilic attacks. Additionally, 2,3-Bis(chloromethyl)-1,4-naphthoquinone may exhibit biological activity, including potential antimicrobial or anticancer properties, although specific biological effects can vary based on the context of use. As with many chlorinated compounds, it is important to handle this substance with care due to potential toxicity and environmental concerns. Proper safety measures should be taken when working with this compound in laboratory settings.
Formula:C12H8Cl2O2
InChI:InChI=1/C12H8Cl2O2/c13-5-9-10(6-14)12(16)8-4-2-1-3-7(8)11(9)15/h1-4H,5-6H2
InChI key:InChIKey=GYYQVIJEJDNZFI-UHFFFAOYSA-N
SMILES:O=C1C=2C(C(=O)C(CCl)=C1CCl)=CC=CC2
Synonyms:
  • 1,4-Naphthalenedione, 2,3-Bis(Chloromethyl)-
  • 1,4-Naphthoquinone, 2,3-bis(chloromethyl)-
  • 2,3-Bis(chloromethyl)-1,4-dihydronaphthalene-1,4-dione
  • 2,3-Bis(chloromethyl)-1,4-naphthalenedione
  • 2,3-Bis(chloromethyl)-1,4-naphthoquinone
  • 2,3-DI(CHLOROMETHYL)-1,4-DIHYDRONAPHTHALENE-1,4-DIONE
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