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| 1H-INDOL-3-OL Basic information |
Product Name: | 1H-INDOL-3-OL | Synonyms: | 3-HYDROXYINDOLE;1,2-Dimethylindole-3-carboxaldehyde;3-Hydroxy-1H-indole;3-Hydroxyindole,97%;1-Boc-1H-Indol-3-ol;RARECHEM AH BS 0105;1,2-DIHYDRO-INDOL-3-ONE;1H-INDOL-3-OL | CAS: | 480-93-3 | MF: | C8H7NO | MW: | 133.15 | EINECS: | | Product Categories: | Indoline & Oxindole | Mol File: | 480-93-3.mol | |
| 1H-INDOL-3-OL Chemical Properties |
Melting point | 85-87 °C | Boiling point | 245.66°C (rough estimate) | density | 1.1475 (rough estimate) | refractive index | 1.5260 (estimate) | storage temp. | Amber Vial, -20°C Freezer, Under inert atmosphere | solubility | DMSO (Slightly), Methanol (Slightly, Sonicated) | pka | 10.10±0.40(Predicted) | form | Solid | color | Dark Green to Black | Stability: | Light Sensitive | CAS DataBase Reference | 480-93-3(CAS DataBase Reference) |
Hazard Codes | Xi | Hazard Note | Irritant | HS Code | 2933998090 |
| 1H-INDOL-3-OL Usage And Synthesis |
Chemical Properties | 1H-INDOL-3-OL is green shiny needles | Uses | 1H-INDOL-3-OL is a mutation product of toluene-4-monooxygenase (T4MO), that gets spontaneously converted to indigo. Used in the preparation of indolyl-oxadiazoles with anticonvulsant activity. | Uses | 3-Hydroxyindole is a mutation product of toluene-4-monooxygenase (T4MO), that gets spontaneously converted to indigo. Used in the preparation of indolyl-oxadiazoles with anticonvulsant activity. | Definition | ChEBI: A member of the class of hydroxyindoles that is 1H-indole substituted by a hydroxy group at position 3. |
| 1H-INDOL-3-OL Preparation Products And Raw materials |
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