5H-quinindoline (CHEM078213)
| Record Information | |||||||||
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| Version | 1.0 | ||||||||
| Creation Date | 2026-04-04 18:50:14 UTC | ||||||||
| Update Date | 2026-04-04 18:50:14 UTC | ||||||||
| Accession Number | CHEM078213 | ||||||||
| Identification | |||||||||
| Common Name | 5H-quinindoline | ||||||||
| Class | Small Molecule | ||||||||
| Description | 5H-quinindoline is an organic compound with the formula C15H10N2 and an average molecular weight of 218.26 g/mol. 5H-quinindoline belongs to the pyrroloquinolines, a subclass of quinolines and derivatives within the organic compounds. This organoheterocyclic compound has been found in or released from one recorded source: electrical and electronic equipment, specifically antennas. | ||||||||
| Contaminant Sources | Not Available | ||||||||
| Contaminant Type | Not Available | ||||||||
| Chemical Structure |  | ||||||||
| Synonyms | Not Available | ||||||||
| Chemical Formula | C15H10N2 | ||||||||
| Average Molecular Mass | 218.259 g/mol | ||||||||
| Monoisotopic Mass | 218.084 g/mol | ||||||||
| CAS Registry Number | 243-38-9 | ||||||||
| IUPAC Name | Not Available | ||||||||
| Traditional Name | Not Available | ||||||||
| SMILES | N1C2=CC=CC=C2C2=CC3=CC=CC=C3N=C12 | ||||||||
| InChI Identifier | InChI=1/C15H10N2/c1-3-7-13-10(5-1)9-12-11-6-2-4-8-14(11)17-15(12)16-13/h1-9H,(H,16,17) | ||||||||
| InChI Key | RDFSPMPXDYGXHP-UHFFFAOYSA-N | ||||||||
| Chemical Taxonomy | |||||||||
| Classification | Not classified | ||||||||
| Biological Properties | |||||||||
| Status | Detected and Not Quantified | ||||||||
| Origin | Not Available | ||||||||
| Cellular Locations | Not Available | ||||||||
| Biofluid Locations | Not Available | ||||||||
| Tissue Locations | Not Available | ||||||||
| Pathways | Not Available | ||||||||
| Applications | Not Available | ||||||||
| Biological Roles | Not Available | ||||||||
| Chemical Roles | Not Available | ||||||||
| Physical Properties | |||||||||
| State | Not Available | ||||||||
| Appearance | Not Available | ||||||||
| Experimental Properties |
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| Predicted Properties | Not Available | ||||||||
| Spectra | |||||||||
| Spectra |
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| Toxicity Profile | |||||||||
| Route of Exposure | Not Available | ||||||||
| Mechanism of Toxicity | Not Available | ||||||||
| Metabolism | Not Available | ||||||||
| Toxicity Values | Not Available | ||||||||
| Lethal Dose | Not Available | ||||||||
| Carcinogenicity (IARC Classification) | Not Available | ||||||||
| Uses/Sources | Not Available | ||||||||
| Minimum Risk Level | Not Available | ||||||||
| Health Effects | Not Available | ||||||||
| Symptoms | Not Available | ||||||||
| Treatment | Not Available | ||||||||
| Concentrations | |||||||||
| Not Available | |||||||||
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| Identifiers | Not Available | ||||||||
| References | |||||||||
| Synthesis Reference | Not Available | ||||||||
| MSDS | Not Available | ||||||||
| General References | Not Available | ||||||||
