P-benzoquinone bis(O-benzoyloxime) (CHEM077741)
| Record Information | |||||||||
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| Version | 1.0 | ||||||||
| Creation Date | 2026-04-04 18:30:21 UTC | ||||||||
| Update Date | 2026-08-20 04:37:23 UTC | ||||||||
| Accession Number | CHEM077741 | ||||||||
| Identification | |||||||||
| Common Name | P-benzoquinone bis(O-benzoyloxime) | ||||||||
| Class | Small Molecule | ||||||||
| Description | P-benzoquinone bis(O-benzoyloxime) is an organic compound with the formula C20H14N2O4 and an average molecular weight of 346.34 g/mol. P-benzoquinone bis(O-benzoyloxime) belongs to the benzoic acids and derivatives, a subclass of benzene and substituted derivatives within the organic compounds. This substance is identified as being found in or released from two recorded sources, specifically antennas and power cables used in electrical and electronic equipment. | ||||||||
| Contaminant Sources | Not Available | ||||||||
| Contaminant Type | Not Available | ||||||||
| Chemical Structure |  | ||||||||
| Synonyms | Not Available | ||||||||
| Chemical Formula | C20H14N2O4 | ||||||||
| Average Molecular Mass | 346.342 g/mol | ||||||||
| Monoisotopic Mass | 346.095 g/mol | ||||||||
| CAS Registry Number | 120-52-5 | ||||||||
| IUPAC Name | [(4-benzoyloxyiminocyclohexa-2,5-dien-1-ylidene)amino] benzoate | ||||||||
| Traditional Name | Not Available | ||||||||
| SMILES | O=C(ON=C1C=CC(C=C1)=NOC(=O)C1=CC=CC=C1)C1=CC=CC=C1 | ||||||||
| InChI Identifier | InChI=1/C20H14N2O4/c23-19(15-7-3-1-4-8-15)25-21-17-11-13-18(14-12-17)22-26-20(24)16-9-5-2-6-10-16/h1-14H | ||||||||
| InChI Key | WMVSVUVZSYRWIY-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 | ||||||||
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| 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 | ||||||||
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| Identifiers | Not Available | ||||||||
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| Synthesis Reference | Not Available | ||||||||
| MSDS | Not Available | ||||||||
| General References | Not Available | ||||||||
