| Weight | 230.219 g/mol |
|---|---|
| Formula | C13H10O4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
2,3,4-Trihydroxybenzophenone (1143-72-2)
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- Positive-working O-quinone diazide photoresist composition with 2,3,4-trihydroxybenzophenone (1987)
- Mechanism of phenolic oxidative coupling reactions. Ferricyanide oxidation of 2,3',4-trihydroxybenzophenone, an example of a radical aromatic substitution mechanism (Journal of the American Chemical Society, 1973)
- Positive photoresist containing 2,3,4-trihydroxybenzophenone and 1,2-naphthoquinone-diazide-5-sulfonyl trisester of 1,3,5-trihydroxybenzene (1991)
- Phenol Dehydrogenations. 12. Oxidative Coupling of 3,5-Dimethyl-2,4,6-trihydroxybenzophenone. (Acta Chemica Scandinavica, 1968)
- ChemInform Abstract: ON THE MECHANISM OF PHENOLIC OXIDATIVE COUPLING REACTIONS, FERRICYANIDE OXIDATION OF 2,3,4-TRIHYDROXYBENZOPHENONE, AN EXAMPLE OF A RADICAL AROMATIC SUBSTITUTION MECHANISM (ChemInform, 1974)
- STUDY ON CATALYTIC SYNTHESIS OF 2,3,4- TRIHYDROXYBENZOPHENONE (Chemistry and Industry of Forest Products, 2002)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)C(=O)C2=C(C(=C(C=C2)O)O)O
-
InChIKeyHTQNYBBTZSBWKL-UHFFFAOYSA-N
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