| Weight | 226.231 g/mol |
|---|---|
| Formula | C14H10O3 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
Xanthene-9-carboxylic acid (82-07-5)
xanthenecarboxylic acid
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- 9H-Xanthene-9-carboxylic acid [1,2,4]oxadiazol-3-yl- and (2H-tetrazol-5-yl)-amides as potent, orally available mGlu1 receptor enhancers (Bioorganic & Medicinal Chemistry Letters, 2005)
- Fluorescein analogue xanthene-9-carboxylic acid: a transition-metal-free CO releasing molecule activated by green light. (Organic Letters, 2013)
- JNJ-20788560 [9-(8-Azabicyclo[3.2.1]oct-3-ylidene)-9H-xanthene-3-carboxylic Acid Diethylamide], a Selective Delta Opioid Receptor Agonist, Is a Potent and Efficacious Antihyperalgesic Agent That Does Not Produce Respiratory Depression, Pharmacologic Tolerance, or Physical Dependence (Journal of Pharmacology and Experimental Therapeutics, 2009)
- Fluorinated 9H-xanthene-9-carboxylic acid oxazol-2-yl-amides as potent, orally available mGlu1 receptor enhancers. (Bioorganic & Medicinal Chemistry Letters, 2009)
- A New Method for Assaying Propantheline and Its Degradation Product, Xanthene-9-carboxylic Acid Using High-Performance Liquid Chromatography (Journal of Pharmaceutical Sciences, 1983)
- Quaternary ammonium salts of heterocyclylalkanol esters of xanthene-9-carboxylic acid (1950)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - xanthenecarboxylic acid
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SMILESC1=CC=C2C(=C1)C(C3=CC=CC=C3O2)C(=O)O
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InChIKeyVSBFNCXKYIEYIS-UHFFFAOYSA-N
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