| Record Information |
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| Version | 1.0 |
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| Creation Date | 2016-05-19 02:42:20 UTC |
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| Update Date | 2016-11-09 01:13:45 UTC |
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| Accession Number | CHEM008270 |
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| Identification |
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| Common Name | Picolinafen |
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| Class | Small Molecule |
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| Description | A pyridinecarboxamide resulting from the formal condensation of the carboxy group of 6-(m-trifluoromethylphenoxy)picolinic acid with the amino group of p-fluoroaniline. A carotenoid biosynthesis inhibitor, it is used as a herbicide for the control of broad-leaved weeds in cereal crops. |
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| Contaminant Sources | - My Exposome Chemicals
- STOFF IDENT Compounds
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| Contaminant Type | Not Available |
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| Chemical Structure | |
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| Synonyms | | Value | Source |
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| 4'-Fluoro-6-(alpha,alpha,alpha-trifluoro-m-tolyloxy)pyridine-2-carboxanilide | ChEBI | | N-(4-Fluorophenyl)-6-[3-(trifluoromethyl)phenoxy]-2-pyridinecarboxamide | ChEBI | | Picolinafene | ChEBI | | 4'-Fluoro-6-(a,a,a-trifluoro-m-tolyloxy)pyridine-2-carboxanilide | Generator | | 4'-Fluoro-6-(α,α,α-trifluoro-m-tolyloxy)pyridine-2-carboxanilide | Generator |
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| Chemical Formula | C19H12F4N2O2 |
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| Average Molecular Mass | 376.311 g/mol |
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| Monoisotopic Mass | 376.083 g/mol |
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| CAS Registry Number | 137641-05-5 |
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| IUPAC Name | N-(4-fluorophenyl)-6-[3-(trifluoromethyl)phenoxy]pyridine-2-carboximidic acid |
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| Traditional Name | N-(4-fluorophenyl)-6-[3-(trifluoromethyl)phenoxy]pyridine-2-carboximidic acid |
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| SMILES | OC(=NC1=CC=C(F)C=C1)C1=NC(OC2=CC=CC(=C2)C(F)(F)F)=CC=C1 |
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| InChI Identifier | InChI=1S/C19H12F4N2O2/c20-13-7-9-14(10-8-13)24-18(26)16-5-2-6-17(25-16)27-15-4-1-3-12(11-15)19(21,22)23/h1-11H,(H,24,26) |
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| InChI Key | CWKFPEBMTGKLKX-UHFFFAOYSA-N |
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| Chemical Taxonomy |
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| Description | belongs to the class of organic compounds known as aromatic anilides. These are aromatic compounds containing an anilide group in which the carboxamide group is substituted with an aromatic group. They have the general structure RNC(=O)R', where R= benzene, and R = aryl group. |
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| Kingdom | Organic compounds |
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| Super Class | Benzenoids |
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| Class | Benzene and substituted derivatives |
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| Sub Class | Anilides |
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| Direct Parent | Aromatic anilides |
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| Alternative Parents | |
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| Substituents | - Aromatic anilide
- Diaryl ether
- Trifluoromethylbenzene
- Pyridine carboxylic acid or derivatives
- Pyridinecarboxamide
- 2-heteroaryl carboxamide
- Phenoxy compound
- Phenol ether
- Fluorobenzene
- Halobenzene
- Aryl fluoride
- Aryl halide
- Pyridine
- Heteroaromatic compound
- Carboxamide group
- Secondary carboxylic acid amide
- Carboxylic acid derivative
- Ether
- Azacycle
- Organoheterocyclic compound
- Organohalogen compound
- Hydrocarbon derivative
- Alkyl halide
- Organic oxide
- Alkyl fluoride
- Organopnictogen compound
- Organic oxygen compound
- Organofluoride
- Organonitrogen compound
- Organooxygen compound
- Organic nitrogen compound
- Aromatic heteromonocyclic compound
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| Molecular Framework | Aromatic heteromonocyclic compounds |
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| External Descriptors | Not Available |
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| Biological Properties |
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| Status | Detected and Not Quantified |
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| Origin | Not Available |
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| Cellular Locations | Not Available |
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| Biofluid Locations | Not Available |
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| Tissue Locations | Not Available |
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| Pathways | Not Available |
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| Applications | Not Available |
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| Biological Roles | Not Available |
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| Chemical Roles | Not Available |
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| Physical Properties |
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| State | Not Available |
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| Appearance | Not Available |
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| Experimental Properties | | Property | Value |
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| Melting Point | Not Available | | Boiling Point | Not Available | | Solubility | Not Available |
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| Predicted Properties | |
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| Spectra |
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| Spectra | | Spectrum Type | Description | Splash Key | View |
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| Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 10V, Positive | splash10-004i-0009000000-0e91df480ada790d1ca5 | Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 20V, Positive | splash10-004i-0219000000-66b111229c51c777d36b | Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 40V, Positive | splash10-0f76-3950000000-254744946198fcbae311 | Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 10V, Negative | splash10-004i-0009000000-f83dc92d3bdc320e4eb8 | Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 20V, Negative | splash10-004i-0129000000-61004ebb4dd85d24aec6 | Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 40V, Negative | splash10-000i-3910000000-031a3508636ddb5adff4 | Spectrum |
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| Toxicity Profile |
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| Route of Exposure | Not Available |
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| Mechanism of Toxicity | Not Available |
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| Metabolism | Not Available |
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| Toxicity Values | Not Available |
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| Lethal Dose | Not Available |
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| Carcinogenicity (IARC Classification) | Not Available |
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| Uses/Sources | Not Available |
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| Minimum Risk Level | Not Available |
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| Health Effects | Not Available |
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| Symptoms | Not Available |
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| Treatment | Not Available |
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| Concentrations |
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| Not Available |
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| External Links |
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| DrugBank ID | Not Available |
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| HMDB ID | Not Available |
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| FooDB ID | Not Available |
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| Phenol Explorer ID | Not Available |
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| KNApSAcK ID | Not Available |
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| BiGG ID | Not Available |
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| BioCyc ID | Not Available |
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| METLIN ID | Not Available |
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| PDB ID | Not Available |
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| Wikipedia Link | Not Available |
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| Chemspider ID | Not Available |
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| ChEBI ID | 138736 |
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| PubChem Compound ID | 3294375 |
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| Kegg Compound ID | Not Available |
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| YMDB ID | Not Available |
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| ECMDB ID | Not Available |
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| References |
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| Synthesis Reference | Not Available |
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| MSDS | Not Available |
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| General References | Not Available |
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