brassicanal A
Identification
| Name | brassicanal A |
| CAS Number | 113866-44-7 |
| FDA UNII | Search |
| Molecular Formula | C9 H7 N O S |
| Molecular Weight | 177.22599000 |
| Nikkaji Number | J423.305K |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Soluble in | water, 186.4 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 brassicanal A usage levels up to | not for fragrance use. |
| Recommendation for brassicanal A flavor usage levels up to | not for flavor use. |
No supplier data available
Potential Uses
Natural Occurrence
Synonyms
2-
methylsulfanyl-1H-indole-3-carbaldehyde
PubMed:
The phytoalexins brassilexin and camalexin inhibit cyclobrassinin hydrolase, a unique enzyme from the fungal pathogen Alternaria brassicicola.
PubMed:
Metabolism of crucifer phytoalexins in Sclerotinia sclerotiorum: detoxification of strongly antifungal compounds involves glucosylation.
PubMed:
Phytoalexins from the crucifer rutabaga: structures, syntheses, biosyntheses, and antifungal activity.
PubMed:
Strategies of cruciferous pathogenic fungi: detoxification of the phytoalexin cyclobrassinin by mimicry.