ChemicalBook--->CAS DataBase List--->59108-90-6

59108-90-6

59108-90-6 Structure

59108-90-6 Structure
IdentificationBack Directory
[Name]

1H-INDOLE-3-CARBOTHIOIC ACID AMIDE
[CAS]

59108-90-6
[Synonyms]

indole-3-thiocarboxamide
1H-Indole-3-carbothioamide
1H-Indole-3-carbothioamide(9CI)
1H-INDOLE-3-CARBOTHIOIC ACID AMIDE
[Molecular Formula]

C9H8N2S
[MDL Number]

MFCD01993552
[MOL File]

59108-90-6.mol
[Molecular Weight]

176.24
Chemical PropertiesBack Directory
[solubility ]

DMF: 30 mg/ml; DMF:PBS(pH 7.2)(1:1): 0.5 mg/ml; DMSO: 20 mg/ml; Ethanol: 20 mg/ml
[form ]

A crystalline solid
[InChI]

1S/C9H8N2S/c10-9(12)7-5-11-8-4-2-1-3-6(7)8/h1-5,11H,(H2,10,12)
[InChIKey]

PPWNZMJWESSLGE-UHFFFAOYSA-N
[SMILES]

NC(=S)c1c[nH]c2ccccc12
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Hazard Codes ]

Xn
[Risk Statements ]

22-43
[Safety Statements ]

36/37
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Skin Sens. 1
Hazard InformationBack Directory
[Uses]

Indole-3-thio carboxamide is an antifungal agent. Indole-3-thio carboxamide is a biotransformation product of Camalexin (HY-119502) by plant pathogenic fungi Botrytis cinerea[1].
[References]

[1] Pedras MS, Abdoli A. Metabolism of the phytoalexins camalexins, their bioisosteres and analogues in the plant pathogenic fungus Alternaria brassicicola. Bioorg Med Chem. 2013 Aug 1;21(15):4541-9. DOI:10.1016/j.bmc.2013.05.026
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