CAS ID | 6093-68-1 |
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IUPAC Name | 6-hydroxychromen-2-one |
Molecular Formula | C9H6O3 |
Molecular Weight | |
SMILES | C1=CC2=C(C=CC(=O)O2)C=C1O |
CAS ID | 6093-68-1 |
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IUPAC Name | 6-hydroxychromen-2-one |
Molecular Formula | C9H6O3 |
Molecular Weight | |
SMILES | C1=CC2=C(C=CC(=O)O2)C=C1O |
99477 |
Synonym: 6-hydroxycoumarin, 6-hydroxy-2h-chromen-2-one, 2h-1-benzopyran-2-one, 6-hydroxy, 6-hydroxycoumaran, 2h-1-benzopyran-2-one,6-hydroxy, 6-hydroxbenzopyran-2-one, 6-hydroxy-2h-chromen-2-on, 6-hydroxycoumarine, 6-hydroxy coumarin, 6-hydroxy-2h-1-benzopyran-2-one
Quantity | 25g |
Melting Point | 249.0°C to 253.0°C |
Infrared Spectrum | Authentic |
Assay Percent Range | 97.5% min. (HPLC) |
Solubility Information | Solubility in water: insoluble. |
Formula Weight | 162.15 |
Percent Purity | 98% |
Chemical Name or Material | 6-Hydroxycoumarin |
6-Hydroxycoumarin, or umbelliferone, is a natural organic compound found in various plants, including chamomile, angelica, and parsley. This lactone derivative of coumarin is widely recognized for its remarkable biological and pharmacological activities.
One of the most notable features of 6-hydroxycoumarin is its fluorescent properties. The compound emits strong fluorescence when exposed to ultraviolet light, which has made it a valuable tool for researchers studying various biological molecules, such as enzymes, nucleic acids, and proteins.
Besides its fluorescence properties, 6-hydroxycoumarin has demonstrated anticoagulant, antioxidant, and anti-inflammatory properties. Traditional medicinal practices have employed this compound to alleviate various health issues, such as skin disorders, inflammation, and pain.
Researchers are now exploring the potential of 6-hydroxycoumarin as a lead compound for developing new drugs. It exhibits the ability to inhibit the growth of cancer cells and possesses neuroprotective properties, which could make it a promising candidate for treating cancer and neurological disorders.
6-hydroxycoumarin is a fascinating compound with diverse biological and pharmacological activities. Its fluorescent properties make it an essential tool for scientific research. At the same time, its potential as a lead compound for drug discovery opens up exciting avenues for developing new therapeutics.
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