5-Formylindole
5-Formylindole
CAS: 1196-69-6
Molecular Formula: C9H7NO
5-Formylindole - Names and Identifiers
| Name | 5-Formylindole |
| Synonyms | 5-Formylindole 5-FORMYLINDOLE 5-Indolealdehyde 5-Indole Aldehyde 5-INDOLE ALDEHYDE INDOLE-5-ALDEHYDE INDOLE-5-CARBALDEHYDE INDOLE-5-CARBOXALDEHYDE Indole-5-carboxaldehyde 1H-indol-5-carbaldehyde 1H-INDOLE-5-CARBALDEHYDE 1H-indole-5-carbaldehyde 1H-indole-6-carbaldehyde 1H-Indole-5-carboxaldehyde 1H-INDOLE-5-CARBOXALDEHYDE |
| CAS | 1196-69-6 |
| EINECS | 627-955-1 |
| InChI | InChI=1/C9H7NO/c11-6-7-1-2-8-3-4-10-9(8)5-7/h1-6,10H |
5-Formylindole - Physico-chemical Properties
| Molecular Formula | C9H7NO |
| Molar Mass | 145.16 |
| Density | 1.278±0.06 g/cm3(Predicted) |
| Melting Point | 100-103°C(lit.) |
| Boling Point | 339.1±15.0 °C(Predicted) |
| Flash Point | 166.8°C |
| Water Solubility | Insoluble in water. |
| Solubility | DMSO, Methanol |
| Vapor Presure | 9.42E-05mmHg at 25°C |
| Appearance | Powder |
| Color | Orange or tan |
| pKa | 16.14±0.30(Predicted) |
| Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
| Sensitive | Air Sensitive |
| Refractive Index | 1.729 |
| MDL | MFCD02093664 |
5-Formylindole - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. |
| WGK Germany | 3 |
| HS Code | 29339900 |
| Hazard Note | Irritant/Keep Cold |
| Hazard Class | IRRITANT |
5-Formylindole - Reference Information
| Uses | Reagents for the preparation of acid yellow derivatives, as anti-proliferation & anti-inflammatory agents; reagents for the preparation of botulinum neurotoxin serum type A protease inhibitors; reagents for the stereoselective synthesis of dibenzylidene acetone derivatives as reagents for β-amyloid imaging probes; reagents for the synthesis of para-para-ostilbene through McMurry coupling reactions; reagents for stereoselective synthesis of heteroaromatic (E)-α,β-unsaturated ketones from aldehydes; reagents for designing aurora kinase A inhibitors in structure-based drugs |
Last Update：2024-04-09 15:16:47
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