| Weight | 162.144 g/mol |
|---|---|
| Formula | C9H6O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
7-hydroxycoumarin (93-35-6)
umbelliferone · 7-hydroxycoumarin sulfate · 7-hydroxycoumarin, 14C-labeled
Score:
#1662 in Biochemistry
,
#3741 in Biology
,
#4710 in Chemistry
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- Brominated 7-hydroxycoumarin-4-ylmethyls: Photolabile protecting groups with biologically useful cross-sections for two photon photolysis (Proceedings of the National Academy of Sciences of the United States of America, 1999)
- Studies in detoxication. 67. The biosynthesis of the glucuronides of umbelliferone and 4-methylumbelliferone and their use in fluorimetric determination of -glucuronidase (Biochemical Journal, 1955)
- ELECTROSTATIC PARAMETERS OF CATIONIC LIPOSOMES COMMONLY USED FOR GENE DELIVERY AS DETERMINED BY 4-HEPTADECYL-7-HYDROXYCOUMARIN (Biochimica et Biophysica Acta, 1997)
- New lanthanide complexes of 4-methyl-7-hydroxycoumarin and their pharmacological activity. (European Journal of Medicinal Chemistry, 2001)
- Studies on the cytostatic and cytotoxic effects and mode of action of 8-nitro-7-hydroxycoumarin (Cancer Letters, 1997)
- pH Effects on fluorescence of umbelliferone (Analytical Chemistry, 1970)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - umbelliferone
- 7-hydroxycoumarin sulfate
- 7-hydroxycoumarin, 14C-labeled
-
SMILESC1=CC(=CC2=C1C=CC(=O)O2)O
-
InChIKeyORHBXUUXSCNDEV-UHFFFAOYSA-N
- Pubchem - 7-hydroxycoumarin
- Wikipedia - umbelliferone
Umbelliferone, also known as 7-hydroxycoumarin, hydrangine, skimmetine, and beta-umbelliferone, is a natural product of the coumarin family. It absorbs ultraviolet light strongly at several wavelengths. Despite several indications that this chemical is photomutagenic, it is used in sunscreens.
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7-hydroxycoumarin
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