2597-03-7
2597-03-7
Chemical Structure
Phenthoate
- CAS No.: 2597-03-7
- Formula:C12H17O4PS2
- Molecular Weight:320.36
IUPAC Name: ethyl 2-((dimethoxyphosphorothioyl)thio)-2-phenylacetate
InChIKey: XAMUDJHXFNRLCY-UHFFFAOYSA-N
SMILES: O=C(OCC)C(SP(OC)(OC)=S)C1=CC=CC=C1
Biological Activity: Phenthoate is an organophosphorus pesticide having low toxicity in animals. Phenthoate is also a AChE inhibitor[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Phenthoate | 98.44% | Phenthoate is an organophosphorus pesticide having low toxicity in animals. Phenthoate is also a AChE inhibitor. | ||||||||||||||||||||
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Phenthoate (Standard) | ≥98% | Phenthoate (Standard) is the analytical standard of Phenthoate. This product is intended for research and analytical applications. Phenthoate is an organophosphorus pesticide having low toxicity in animals. Phenthoate is also a AChE inhibitor. | ||||||||||||||||||||
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Phenthoate-d6 | Phenthoate-d6 is deuterium labeled Phenthoate. Phenthoate is an organophosphorus pesticide having low toxicity in animals. Phenthoate is also a AChE inhibitor. | |||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.61
HY-129518Phenamacide hydrochloride -
Similarity Score 0.61
HY-W006062H-Phg-OtBu.HCl -
Similarity Score 0.61
HY-W042009A(R)-Phenylglycine tert-butyl ester hydrochloride -
Similarity Score 0.61
HY-77721Diethyl benzylmalonate -
Similarity Score 0.60
HY-B1574Butetamate -
Similarity Score 0.60
HY-W013416(R)-Ethyl 2-amino-4-phenylbutanoate hydrochloride -
Similarity Score 0.60
HY-130960Tubulysin IM-3 -
Similarity Score 0.60
HY-B0184AFelbamate hydrate -
Similarity Score 0.59
HY-B1863RIprobenfos (Standard) -
Explore the MedChemAI to find more analogs
References
- [1]. Akina Nara, et al. Fatal Poisoning With Both Dichlorvos and Phenthoate. J Forensic Sci. 2018 Nov;63(6):1928-1931. [Content Brief]
- [2]. Fei Ding, et al. Elucidating the Potential Neurotoxicity of Chiral Phenthoate: Molecular Insight From Experimental and Computational Studies. Chemosphere. 2020 Sep;255:127007. [Content Brief]
