nardofuran
12-hydroxy-2,3,11,11-tetramethyl-10-oxatricyclo[7.2.1.02,7]dodec-6-en-8-one
Identification
| Name | nardofuran |
| CAS Number | 42438-76-6 |
| FDA UNII | Search |
| Molecular Formula | C15 H22 O3 |
| Molecular Weight | 250.33794000 |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 389.82 °C. @ 760.00 mm Hg (est) |
| Flash Point | 289.00 °F. TCC ( 142.80 °C. ) (est) |
| logP (o/w) | 2.320 (est) |
| Soluble in | water, 49.4 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| 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 nardofuran usage levels up to | not for fragrance use. |
| Recommendation for nardofuran flavor usage levels up to | not for flavor use. |
No supplier data available
Potential Uses
Natural Occurrence
Synonyms
12-
hydroxy-2,3,11,11-tetramethyl-10-oxatricyclo[7.2.1.02,7]dodec-6-en-8-one
1,4-
methano-3-benzoxepin-5(4H)-one, 1,2,7,8,9,9a-hexahydro-10-hydroxy-2,2,9,9a-tetramethyl-, (1S-(1a,4a,9a,9aa,10R*))-
(1S-(1alpha,4alpha,9alpha,9aalpha,10R*))-1,2,7,8,9,9a-
nardofuran
nardofurane
PubMed:
Effect of artemisinin/artesunate as inhibitors of hepatitis B virus production in an "in vitro" replicative system.
PubMed:
Activity of drugs from traditional Chinese medicine toward sensitive and MDR1- or MRP1-overexpressing multidrug-resistant human CCRF-CEM leukemia cells.
PubMed:
[The constitution of allylic oxidation products of nardofuran (author's transl)].