| Identification | Back Directory | [Name]
pyrisoxazole | [CAS]
847749-37-5 | [Synonyms]
pyrisoxazole
pyrisoxazole Solution, 1000ppm
Pyrisoxazole Solution in Methanol, 100μg/mL
Pyridine, 3-[5-(4-chlorophenyl)-2,3-dimethyl-3-isoxazolidinyl]- | [Molecular Formula]
C16H17ClN2O | [MDL Number]
MFCD32874250 | [MOL File]
847749-37-5.mol | [Molecular Weight]
288.77 |
| Chemical Properties | Back Directory | [Melting point ]
54 - 56°C | [Boiling point ]
401.4±55.0 °C(Predicted) | [density ]
1.189±0.06 g/cm3(Predicted) | [storage temp. ]
Amber Vial, Refrigerator | [solubility ]
Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly) | [form ]
Solid | [pka]
4.91±0.12(Predicted) | [color ]
Pale Yellow to Light Yellow Thick Oil to | [Stability:]
Light Sensitive |
| Hazard Information | Back Directory | [Uses]
Pyrisoxazole is a novel fungicide, inhibitor of Sterol 14α-demethylase. | [Definition]
ChEBI: 3-[5-(4-chlorophenyl)-2,3-dimethyl-1,2-oxazolidin-3-yl]pyridine is a member of the class of oxazolidines that is 2,3-dimethyl-1,2-oxazolidine carrying additional 3-pyridyl and 4-chlorophenyl substituents at positions 3 and 5 respectively. It is a member of pyridines, a member of oxazolidines and a member of monochlorobenzenes. | [Production Methods]
Pyrisoxazole is produced commercially through a multi-step synthesis that constructs its isoxazole fungicide framework by coupling a chloropyridyl fragment with a methoxy-substituted isoxazole moiety. Industrial production begins with the preparation of the 3,5-dichloropyridin-2-yl intermediate, which undergoes etherification with a benzyl alcohol derivative. In parallel, the isoxazole ring is formed via cyclisation of a diketone precursor with hydroxylamine. These fragments are then joined through an oxymethyl linkage to yield the final structure. | [Mechanism of action]
Sterol biosynthesis inhibitor | [Pesticide Type]
Fungicide |
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TargetMol
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400-821-0310 15002144251 |
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www.targetmol.cn/ |
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