| Weight | 162.144 g/mol |
|---|---|
| Formula | C9H6O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
4-Hydroxycoumarin (1076-38-6, 22105-09-5)
4-OH coumarin
Score:
#1841 in Biochemistry
,
#5020 in Chemistry
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- Sigma-Aldrich - 4-Hydroxycoumarin47.30 - 179.00 USD
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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)
- Novel 4-hydroxycoumarin anticoagulants active against resistant rats. (Nature, 1975)
- 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)
- Heteroaromatization with 4-Hydroxycoumarin Part II: Synthesis of Some New Pyrano[2,3-d]pyrimidines, [1,2,4]triazolo[1,5-c]pyrimidines and Pyrimido[1,6-b]-[1,2,4]triazine Derivatives (Molecules, 2001)
- 4-Hydroxycoumarin in heterocyclic synthesis: Part III. Synthesis of some new pyrano[2,3-d]pyrimidine, 2-substituted[1,2,4]triazolo[1,5-c]pyrimidine and pyrimido[1,6-b][1,2,4]triazine derivatives (Farmaco, 2000)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 4-OH coumarin
-
SMILESC1=CC=C2C(=C1)C(=CC(=O)O2)O
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InChIKeyVXIXUWQIVKSKSA-UHFFFAOYSA-N
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