Benzodioxan

Source: Wikipedia, the free encyclopedia.
1,4-Benzodioxan
Names
Preferred IUPAC name
2,3-Dihydro-1,4-benzodioxine
Other names
Dihydrobenzodioxin; 1,4-Benzodioxane; Benzo-1,4-dioxane; Ethylene o-phenylene dioxide; Pyrocatechol ethylene ether
Identifiers
3D model (
JSmol
)
ChemSpider
UNII
  • InChI=1S/C8H8O2/c1-2-4-8-7(3-1)9-5-6-10-8/h1-4H,5-6H2
    Key: BNBQRQQYDMDJAH-UHFFFAOYSA-N
  • InChI=1/C8H8O2/c1-2-4-8-7(3-1)9-5-6-10-8/h1-4H,5-6H2
    Key: BNBQRQQYDMDJAH-UHFFFAOYAF
  • c1ccc2c(c1)OCCO2
Properties
C8H8O2
Molar mass 136.150 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

The benzodioxans are a group of

1,4-dioxane, which respectively give 1,2-benzodioxan, 1,3-benzodioxan and 1,4-benzodioxan.[2][3]

Derivatives

Some derivatives of 1,4-benzodioxan are used as pharmaceuticals including:[4][5][6][7]

See also

References

  1. National Library of Medicine. Archived
    from the original on 2022-09-05. Retrieved 2022-09-05.
  2. ^ "TECHNICAL FACT SHEET – 1,4-DIOXANE" (PDF). Technical Fact Sheet. 51 (6): 9. 2017. Archived (PDF) from the original on 2022-08-13. Retrieved 2022-09-05 – via United States Environmental Protection Agency.
  3. United States Department of Health
    .
  4. PMID 21782456
    .
  5. ^ "1,4-benzodioxan derivatives their preparation and pharmaceutical compositions containing them - Patent IL-43272-A - PubChem". pubchem.ncbi.nlm.nih.gov. Retrieved 2022-09-05.
  6. PMID 27658794
    .
  7. PMID 18683910
    .

External links


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