Weight | 184.194 g/mol |
---|---|
Formula | C12H8O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 2 |
Rotatable Bonds | 0 |
Oxanthrene (262-12-4)
dibenzo(1,4)dioxin · dibenzo-p-dioxin
Score:
#162 in Environmental science
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#2362 in Biology
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#2926 in Chemistry
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- Potencies of polychlorinated dibenzo-p-dioxin, dibenzofuran, and biphenyl congeners, relative to 2,3,7,8-tetrachlorodibenzo-p-dioxin, for producing early life stage mortality in rainbow trout (Oncorhynchus mykiss) (Aquatic Toxicology, 1991)
- Metabolism of dibenzo-p-dioxin by Sphingomonas sp. strain RW1. (Applied and Environmental Microbiology, 1992)
- Identification of polychlorinated dibenzo-p-dioxin isomers found in fly ash (Chemosphere, 1978)
- Model studies of polychlorinated dibenzo-p-dioxin formation during municipal refuse incineration (Science, 1987)
- Chemical and toxicological evaluations of isolated and synthetic chloro derivatives of dibenzo-p-dioxin. (Nature, 1968)
- Microbial degradation of dibenzofuran, fluorene, and dibenzo-p-dioxin by staphylococcus auriculans DBF63 (Applied and Environmental Microbiology, 1993)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - dibenzo(1,4)dioxin
- dibenzo-p-dioxin
-
SMILESC1=CC=C2C(=C1)OC3=CC=CC=C3O2
-
InChIKeyNFBOHOGPQUYFRF-UHFFFAOYSA-N
- Pubchem - Oxanthrene
- Wikipedia - dibenzo-p-dioxin
Dibenzo-1,4-dioxin, also dibenzodioxin or dibenzo-p-dioxin (dibenzo-para-dioxin), is a polycyclic heterocyclic organic compound in which two benzene rings are connected by a 1,4-dioxin ring. Its molecular formula is C12H8O2. The two oxygen atoms occupy opposite (para-) positions in the six-membered dioxin ring.
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