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analytical standard Analytical standard for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Sonrisas canónicas | COP(=S)(OC)OC1=CC(=C(C=C1Cl)Br)Cl |
|---|---|
| IUPAC Name | (4-bromo-2,5-dichlorophenoxy)-dimethoxy-sulfanylidene-λ5-phosphane |
| InChIKey | NYQDCVLCJXRDSK-UHFFFAOYSA-N |
| INCHI | 1S/C8H8BrCl2O3PS/c1-12-15(16,13-2)14-8-4-6(10)5(9)3-7(8)11/h3-4H,1-2H3 |
| Isómeros SMILES | COP(=S)(OC)OC1=CC(=C(C=C1Cl)Br)Cl |
| WGK Alemania | 3 |
| RTECS | TE7175000 |
| Número ONU | 3077 |
| Peso molecular | 366 |
| Beilstein | 1988276 |
| Reaxy-Rn | 1988276 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1988276&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Clase | Organic thiophosphoric acids and derivatives |
| Subclass | Thiophosphoric acid esters |
| Intermediate Tree Nodes | Aryl thiophosphates |
| Direct Parent | Phenyl thiophosphates |
| Alternative Parents | Thiophosphate triesters Phenoxy compounds Dichlorobenzenes Bromobenzenes Aryl chlorides Aryl bromides Organooxygen compounds Organochlorides Organobromides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Phenyl thiophosphate - Phenoxy compound - 1,4-dichlorobenzene - Thiophosphate triester - Bromobenzene - Chlorobenzene - Halobenzene - Aryl bromide - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Hydrocarbon derivative - Organic oxygen compound - Organooxygen compound - Organohalogen compound - Organobromide - Organochloride - Aromatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as phenyl thiophosphates. These are organothiophosphorus compounds that contain a thiophosphoric acid O-esterified with a phenyl group. |
| External Descriptors | Organophosphorus insecticides |
| Solubilidad | Slightly soluble in water, soluble in benzene, ether, and carbon tetrachloride. |
|---|---|
| Punto de inflamación (°F) | >100 °C |
| Punto de inflamación (°C) | >100°C |
| Peso molecular | 366.000 g/mol |
| XLogP3 | 5.200 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 4 |
| Exact Mass | 363.849 Da |
| Monoisotopic Mass | 363.849 Da |
| Topological Polar Surface Area | 59.800 Ų |
| Heavy Atom Count | 16 |
| Formal Charge | 0 |
| Complexity | 276.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Linfeng Chen, Xike Tian, Yong Li, Liqiang Lu, Yulun Nie, Yanxin Wang. (2020) Broad-spectrum pesticide screening by multiple cholinesterases and thiocholine sensors assembled high-throughput optical array system. JOURNAL OF HAZARDOUS MATERIALS, [PMID:33254811] [10.1016/j.jhazmat.2020.123830] |
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