Abstract

In the title compound, C10H13NO2S, the thio­phene and isoxazoline rings are almost coplanar, the dihedral angle between their least-squares planes being 2.08 (1)°. The O—H atoms of the methyl hy­droxy group and the N atom of the isoxazole ring are orientated in the same direction to allow for the formation of inter­molecular O—H⋯N hydrogen bonds that lead to a supra­molecular chain along the a axis.

Highlights

  • In the title compound, C10H13NO2S, the thiophene and isoxazoline rings are almost coplanar, the dihedral angle between their least-squares planes being 2.08 (1)

  • Atoms of the methyl hydroxy group and the N atom of the isoxazole ring are orientated in the same direction to allow for the formation of intermolecular O—H N hydrogen bonds that lead to a supramolecular chain along the a axis

  • R-factors based on F2 are statistically about twice as large as those based on F, and R- factors based on ALL data will be even larger

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Summary

Bruker APEXII CCD diffractometer

Jae Choon Woob and Chong-Hyeak Kimc a Biomaterials Research Center, Korea Research Institute of Chemical Technology, PO. R factor = 0.047; wR factor = 0.149; data-to-parameter ratio = 20.6. C10H13NO2S, the thiophene and isoxazoline rings are almost coplanar, the dihedral angle between their least-squares planes being 2.08 (1). The O—H atoms of the methyl hydroxy group and the N atom of the isoxazole ring are orientated in the same direction to allow for the formation of intermolecular O—H N hydrogen bonds that lead to a supramolecular chain along the a axis. KEIT [10035240, Development of new herbicides for resistant weeds with mutated genes]

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