1H-INDOLE-3-CARBOTHIOIC ACID AMIDE
- Product Name
- 1H-INDOLE-3-CARBOTHIOIC ACID AMIDE
- CAS No.
- 59108-90-6
- Chemical Name
- 1H-INDOLE-3-CARBOTHIOIC ACID AMIDE
- Synonyms
- indole-3-thiocarboxamide;1H-Indole-3-carbothioamide;1H-Indole-3-carbothioamide(9CI);1H-INDOLE-3-CARBOTHIOIC ACID AMIDE
- CBNumber
- CB6369752
- Molecular Formula
- C9H8N2S
- Formula Weight
- 176.24
- MOL File
- 59108-90-6.mol
1H-INDOLE-3-CARBOTHIOIC ACID AMIDE Property
- 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
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P405Store locked up.
N-Bromosuccinimide Price
- Product number
- 11065
- Product name
- Indole-3-thio Carboxamide
- Purity
- ≥97%
- Packaging
- 250mg
- Price
- $93
- Updated
- 2024/03/01
- Product number
- 11065
- Product name
- Indole-3-thio Carboxamide
- Purity
- ≥97%
- Packaging
- 1g
- Price
- $330
- Updated
- 2024/03/01
- Product number
- 11065
- Product name
- Indole-3-thio Carboxamide
- Purity
- ≥97%
- Packaging
- 500mg
- Price
- $176
- Updated
- 2024/03/01
- Product number
- I655750
- Product name
- 1H-Indole-3-carbothioicAcidAmide
- Packaging
- 500mg
- Price
- $200
- Updated
- 2021/12/16
- Product number
- CHM0313315
- Product name
- 1H-INDOLE-3-CARBOTHIOIC ACID AMIDE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $504.39
- Updated
- 2021/12/16
1H-INDOLE-3-CARBOTHIOIC ACID AMIDE Chemical Properties,Usage,Production
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
1H-INDOLE-3-CARBOTHIOIC ACID AMIDE Preparation Products And Raw materials
Raw materials
Preparation Products
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