4,7-dihydroxycoumarin
2H-1-benzopyran-2-one, 4,7-dihydroxy-
Identification
| Name | 4,7-dihydroxycoumarin |
| CAS Number | 1983-81-9 |
| FDA UNII | Search |
| Molecular Formula | C9 H6 O4 |
| Molecular Weight | 178.14362000 |
| MDL Number | MFCD00203882 |
| Nikkaji Number | J80.358H |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Soluble in | water, 1.6e+005 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Preferred SDS | View |
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | natural substances and extractives |
| Recommendation for 4,7-dihydroxycoumarin usage levels up to | not for fragrance use. |
| Recommendation for 4,7-dihydroxycoumarin flavor usage levels up to | not for flavor use. |
BOC Sciences
Best of Chemicals Supplier
Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecul...
Potential Uses
Natural Occurrence
Synonyms
2H-1-
benzopyran-2-one, 4,7-dihydroxy-
4,7-
dihydroxy-2H-1-benzopyran-2-one
4,7-
dihydroxychromen-2-one
PubMed:
Origin of Remarkably Different Acidity of Hydroxycoumarins-Joint Experimental and Theoretical Studies.
PubMed:
New aminocoumarins from the rare actinomycete Catenulispora acidiphila DSM 44928: identification, structure elucidation, and heterologous production.
PubMed:
Formation of coumarines during the degradation of alkyl substituted aromatic oil components by the yeast Trichosporon asahii.
PubMed:
Antimicrobial and DNA gyrase-inhibitory activities of novel clorobiocin derivatives produced by mutasynthesis.
PubMed:
Coumarin-based inhibitors of HIV integrase.