protoillud-6-ene
6-protoilludene
Identification
| Name | protoillud-6-ene |
| IUPAC | (4aS,7aS,7bR)-3,6,6,7b-tetramethyl-2,4,4a,5,7,7a-hexahydro-1H-cyclobuta[e]indene |
| Molecular Formula | C15 H24 |
| Molecular Weight | 204.35628000 |
| Nikkaji Number | J1.049.581D |
| Beilstein | 4383202 |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Soluble in | water, 0.2284 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 protoillud-6-ene usage levels up to | not for fragrance use. |
| Recommendation for protoillud-6-ene flavor usage levels up to | not for flavor use. |
No supplier data available
Potential Uses
Natural Occurrence
Synonyms
6-
protoilludene
(4aS,7aS,7bR)-3,6,6,7b-
tetramethyl-2,4,4a,5,7,7a-hexahydro-1H-cyclobuta[e]indene
PubMed:
Moonlighting Metals: Insights into Regulation of Cyclization Pathways in Fungal Î(6) -Protoilludene Sesquiterpene Synthases.
PubMed:
Chemodiversity and biodiversity of fungi associated with the pine weevil Hylobius abietis.
PubMed:
Cloning and characterization of an Armillaria gallica cDNA encoding protoilludene synthase, which catalyzes the first committed step in the synthesis of antimicrobial melleolides.