
1-(2-fluoro-3-methylphenyl)-2-pyridin-4-ylethanone (CHEM177492)
| Record Information | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Version | 1.0 | ||||||||
| Creation Date | 2026-08-19 04:40:29 UTC | ||||||||
| Update Date | 2026-08-19 04:40:29 UTC | ||||||||
| Accession Number | CHEM177492 | ||||||||
| Identification | |||||||||
| Common Name | 1-(2-fluoro-3-methylphenyl)-2-pyridin-4-ylethanone | ||||||||
| Class | Small Molecule | ||||||||
| Description | 1-(2-fluoro-3-methylphenyl)-2-pyridin-4-ylethanone belongs to the carbonyl compounds, a subclass of organooxygen compounds within the organic compounds. This compound has the formula C14H12FNO and an average molecular weight of 229.25 g/mol. It is further classified under the superclass of organic oxygen compounds and the class of organooxygen compounds. | ||||||||
| Contaminant Sources | Not Available | ||||||||
| Contaminant Type | Not Available | ||||||||
| Chemical Structure | |||||||||
| Synonyms | Not Available | ||||||||
| Chemical Formula | C14H12FNO | ||||||||
| Average Molecular Mass | 229.250 g/mol | ||||||||
| Monoisotopic Mass | 229.090 g/mol | ||||||||
| CAS Registry Number | 1504551-75-0 | ||||||||
| IUPAC Name | 1-(2-fluoro-3-methylphenyl)-2-pyridin-4-ylethanone | ||||||||
| Traditional Name | Not Available | ||||||||
| SMILES | Not Available | ||||||||
| InChI Identifier | InChI=1S/C14H12FNO/c1-10-3-2-4-12(14(10)15)13(17)9-11-5-7-16-8-6-11/h2-8H,9H2,1H3 | ||||||||
| InChI Key | PZUVEIPVEVOPNP-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 |
| ||||||||
| Predicted Properties | Not Available | ||||||||
| Spectra | |||||||||
| Spectra |
| ||||||||
| 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 | |||||||||
| External Links | |||||||||
| Identifiers | Not Available | ||||||||
| References | |||||||||
| Synthesis Reference | Not Available | ||||||||
| MSDS | Not Available | ||||||||
| General References | Not Available | ||||||||