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Kresoxim-methyl derivatives (Cao et al., 2017) are broad-spectrum fungicides (e.g., Grossmann & Retzlaff, 1997), have a site-specific action (Olaya et al., 1998) and high efficiency (Patel et al., 2012) against various diseases of agricultural crops (Balba, 2007). As these types of compounds are easily metabolized in nature as well as in living systems, their modifications are of importance in order to improve their activity (Balba, 2007). In order to increase the activity of the starting compounds (Kant et al. 2012), it is necessary to modify the basic skeleton and initiate a structural investigation of different derivatives of kresoxim-methyl derivatives and in that light we previously reported the crystal structure of a related derivative, (2E)-2-methoxyimino-2-{2-[(2-methylphenoxy)methyl]phenyl}-N0-(4-nitrobenzylidene)ethanohydrazide (Shripanavar & Butcher, 2015). This paper is a continuation in this series. The title compound crystallizes with two molecules, A and B, in the asymmetric unit, as shown in Fig. 1. Both molecules exhibit similar conformations. For molecule A, the central ethane hydrazide moiety N2A/N3A/C17A/O3A is close to planar with an r.m.s. deviation of 0.02 Å for the fitted atoms. The dihedral angles between these atoms and the adjacent rings are 17.1 (2) (C19A methoxyphenyl ring) and 79.9 (2) (C14A benzene Received 28 July 2020 Accepted 1 August 2020

(Z)-N′-[(E)-4-Methoxybenzylidene]-2-(methoxyimino)-2-{2-[(2-methylphenoxy)methyl]phenyl}acetohydrazide