| Weight | 296.433 g/mol |
|---|---|
| Formula | C7H3Cl5S |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
Pentachlorothioanisole (1825-19-0)
PCTA compound · pentachloromethylthiobenzene · methylthiopentachlorobenzene
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- In vitro metabolism of pentachloronitrobenzene to pentachloromethylthiobenzene by onion: Characterization of glutathione S-transferase, cysteine C-S lyase, and S-adenosylmethionine methyl transferase activities (Pesticide Biochemistry and Physiology, 1980)
- The metabolism of pentachloromethylthiobenzene in germ-free and conventional rats (Xenobiotica, 1981)
- Biliary excretion and intestinal metabolism in the intermediary metabolism of pentachlorothioanisole (Xenobiotica, 1990)
- Formation of pentachlorothioanisole from N-acetyl-S-(pentachlorophenyl) cysteine in blood and liver of rats in vivo (Life Sciences, 1983)
- Glutathione-S-transferase-mediated methylthio displacement and turnover in the metabolism of pentachlorothioanisole by rats. (Xenobiotica, 1991)
- Glutathione-mediated methylthio-turnover and sex differences in the metabolism of pentachlorothioanisole by rat. (Xenobiotica, 1993)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - PCTA compound
- pentachloromethylthiobenzene
- methylthiopentachlorobenzene
-
SMILESCSC1=C(C(=C(C(=C1Cl)Cl)Cl)Cl)Cl
-
InChIKeyLGZZJTIUEJNNKV-UHFFFAOYSA-N
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Pentachlorothioanisole
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