Weight | 170.211 g/mol |
---|---|
Formula | C12H10O |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 2 |
Rotatable Bonds | 2 |
Diphenyl oxide (101-84-8)
phenyl ether · diphenyl ether
Score:
#395 in Physics
,
#1042 in Biology
,
#1163 in Chemistry
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- Detailed polybrominated diphenyl ether (PBDE) congener composition of the widely used penta-, octa-, and deca-PBDE technical flame-retardant mixtures. (Environmental Science & Technology, 2006)
- Polybrominated diphenyl ether (PBDE) flame retardants. (Science of The Total Environment, 2001)
- DEVELOPMENTAL NEUROTOXICITY OF POLYBROMINATED DIPHENYL ETHER (PBDE) FLAME RETARDANTS (Neurotoxicology, 2007)
- Polybrominated diphenyl ether flame retardants in the North American environment (Environment International, 2003)
- Catalytic activity of various salts in the reaction of 2,3-epoxypropyl phenyl ether and carbon dioxide under atmospheric pressure (Journal of Organic Chemistry, 1993)
- Design, synthesis, and DNA binding properties of bifunctional intercalators. Comparison of polymethylene and diphenyl ether chains connecting phenanthridine (Journal of the American Chemical Society, 1985)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H360: May damage fertility or the unborn child
Danger Reproductive toxicity - Category 1A, 1B - H400: Very toxic to aquatic life
Warning Hazardous to the aquatic environment, acute hazard - Category 1 - phenyl ether
- diphenyl ether
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SMILESC1=CC=C(C=C1)OC2=CC=CC=C2
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InChIKeyUSIUVYZYUHIAEV-UHFFFAOYSA-N
- Pubchem - Diphenyl oxide
- Wikipedia - diphenyl ether
Diphenyl ether is the organic compound with the formula O(C6H5)2. The molecule is subject to reactions typical of other phenyl rings, including hydroxylation, nitration, halogenation, sulfonation, and FriedelCrafts alkylation or acylation. This simple diaryl ether enjoys a variety of niche applications.
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