Cas no 3067-10-5 (7-Hydroxy-5-methoxycoumarin)
7-Hydroxy-5-methoxycoumarin structure
Product Name:7-Hydroxy-5-methoxycoumarin
CAS No:3067-10-5
MF:C10H8O4
MW:192.168123245239
CID:316216
PubChem ID:5487854
Update Time:2025-04-19
7-Hydroxy-5-methoxycoumarin Chemical and Physical Properties
Names and Identifiers
-
- 2H-1-Benzopyran-2-one,7-hydroxy-5-methoxy-
- 5-Methoxy-7-hydroxycoumarin
- 2H-1-Benzopyran-2-one,7-hydroxy-5-methoxy
- 7-Hydroxy-5-methoxy-2H-1-benzopyran-2-one
- 7-hydroxy-5-methoxy-chromen-2-one
- 7-hydroxy-5-methoxychromene-2-one
- 7-hydroxy-5-methoxycoumarin
- 7-Hydroxy-5-methoxy-cumarin
- 2H-1-Benzopyran-2-one, 7-hydroxy-5-methoxy-
- 7-Hydroxy-5-methoxy-2H-chromen-2-on
- 7-Hydroxy-5-methoxy-2H-chromen-2-one
- 7-Hydroxy-5-méthoxy-2H-chromén-2-one
- 7-hydroxy-5-methoxychromen-2-one
- 5-Methoxy-7-hydroxy-2H-1-benzopyran-2-one
- CHEMBL449529
- AKOS022643896
- 3067-10-5
- SCHEMBL7837457
- DTXSID30184706
- FS-7860
- 7-Hydroxy-5-methoxycoumarin
-
- Inchi： 1S/C10H8O4/c1-13-8-4-6(11)5-9-7(8)2-3-10(12)14-9/h2-5,11H,1H3
- InChI Key： IFIRYJJHHOCCHT-UHFFFAOYSA-N
- SMILES： O1C(C=CC2C(=CC(=CC1=2)O)OC)=O
Computed Properties
- Exact Mass: 192.04200
- Monoisotopic Mass: 192.042259
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 14
- Rotatable Bond Count: 1
- Complexity: 261
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 55.8
- XLogP3: 1.5
Experimental Properties
- Color/Form: Powder
- Density: 1.377
- Boiling Point: 429.9°Cat760mmHg
- Flash Point: 179.6°C
- Refractive Index: 1.609
- PSA: 59.67000
- LogP: 1.50720
7-Hydroxy-5-methoxycoumarin Related Literature
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Nigel C. Veitch Nat. Prod. Rep. 2013 30 988
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2. Formula index
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Wei Li,Jun-Sheng Zhang,Jia-Luo Huang,Min-Hong Jiang,You-Kai Xu,Abrar Ahmed,Sheng Yin,Gui-Hua Tang RSC Adv. 2017 7 31061
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4. Synthesis of the Mammea coumarins. Part 2. Experiments in the mammea E series and synthesis of mammea E/ACLeslie Crombie,Raymond C. F. Jones,Christopher J. Palmer J. Chem. Soc. Perkin Trans. 1 1987 333
-
William N. Howell,Alexander Robertson J. Chem. Soc. 1937 293
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