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| (aR,)-rel-a-tert-Butyl-b-(4-chlorophenoxy)-1H-1,2,4-triazole-1-ethanol PESTANAL Basic information |
Product Name: | (aR,)-rel-a-tert-Butyl-b-(4-chlorophenoxy)-1H-1,2,4-triazole-1-ethanol PESTANAL | Synonyms: | (αR,βS)-rel-α-tert-Butyl-β-(4-chlorophenoxy)-1H-1,2,4-triazole-1-ethanol;(aR,)-rel-a-tert-Butyl-b-(4-chlorophenoxy)-1H-1,2,4-triazole-1-ethanol PESTANAL;1H-1,2,4-Triazole-1-ethanol, β-(4-chlorophenoxy)-α-(1,1-dimethylethyl)-, (αR,βS)-rel- | CAS: | 70585-35-2 | MF: | C14H18ClN3O2 | MW: | 295.76 | EINECS: | | Product Categories: | | Mol File: | 70585-35-2.mol | |
| (aR,)-rel-a-tert-Butyl-b-(4-chlorophenoxy)-1H-1,2,4-triazole-1-ethanol PESTANAL Chemical Properties |
Boiling point | 465.4±55.0 °C(Predicted) | density | 1.24±0.1 g/cm3(Predicted) | Fp | 100 °C | pka | 13.29±0.20(Predicted) | form | neat |
Hazard Codes | Xn | Risk Statements | 22-52/53 | Safety Statements | 61 | WGK Germany | 2 |
| (aR,)-rel-a-tert-Butyl-b-(4-chlorophenoxy)-1H-1,2,4-triazole-1-ethanol PESTANAL Usage And Synthesis |
Uses | Triadimenol A is a fungicide and is formed through the enantioselective degradation, abiotic racemization, and chiral transformation of triadimefon in soils. |
| (aR,)-rel-a-tert-Butyl-b-(4-chlorophenoxy)-1H-1,2,4-triazole-1-ethanol PESTANAL Preparation Products And Raw materials |
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