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C 12 H 10 N 2 O 2 ,monoclinic, P2 1 /c (no. 14), a =12.294 (3) Source of material Reagents and solvents used were of commercially available quality. Thet itle compound was prepared according to reported precedures [11, 12] .Dropwise addition of cyclopropanecarbonyl chloride to (Z)-N-hydroxybenzimidoyl cyanide (7.50 mmol in 25 mL THF) and 7.5mmolEt 3 N, then vigorously stirred at ambient temperature for 12h. The corresponding product precipitated immediately. Thetitle compound was dissolved indoi:10.1524/ncrs.2013.0043 fatcat:puaoou7jhzdbzoodhkb7nu2kx4