Abstract

In the asymmetric unit of the title compound {systematic name: N′-(2,4-di­methyl­phen­yl)-N-[N-(2,4-di­methyl­phen­yl)carbox­imido­yl]-N-methyl­methanimidamide}, C19H23N3, which is a formamidine pesticide, there are two independent and conformationally similar mol­ecules, with the dihedral angle between the mean planes of the 2,4-di­methylbenzene rings in each mol­ecule being 41.63 (6) and 42.09 (5)°. The crystal structure is stabilized by a C—H⋯N hydrogen bond, as well as weak inter­molecular C—H⋯π and π–π inter­actions [ring centroid separation = 3.7409 (15) Å], giving one-dimensional chains extending down the b direction.

Highlights

  • In the asymmetric unit of the title compound {systematic name: N0 -(2,4-dimethylphenyl)-N-[N-(2,4-dimethylphenyl)carboximidoyl]-N-methylmethanimidamide}, C19H23N3, which is a formamidine pesticide, there are two independent and conformationally similar molecules, with the dihedral angle between the mean planes of the 2,4-dimethylbenzene rings in each molecule being 41.63 (6) and 42.09 (5)

  • The crystal structure is stabilized by a C—H N hydrogen bond, as well as weak intermolecular C—H and – interactions [ring centroid separation = 3.7409 (15) Å], giving one-dimensional chains extending down the b direction

  • All bond lengths and bond angles are normal and comparable to those observed in the crystal structures of a similar compound (Peoples et al, 2012)

Read more

Summary

Jeona and Jineun Kima*

R factor = 0.062; wR factor = 0.182; data-to-parameter ratio = 16.2. Cg1 and Cg4 are the centroids of the C2–C8 and C31–C38 rings. In the asymmetric unit of the title compound {systematic name: N0 -(2,4-dimethylphenyl)-N-[N-(2,4-dimethylphenyl)carboximidoyl]-N-methylmethanimidamide}, C19H23N3, which is a formamidine pesticide, there are two independent and conformationally similar molecules, with the dihedral angle between the mean planes of the 2,4-dimethylbenzene rings in each molecule being 41.63 (6) and 42.09 (5). The crystal structure is stabilized by a C—H N hydrogen bond, as well as weak intermolecular C—H and – interactions [ring centroid separation = 3.7409 (15) Å], giving one-dimensional chains extending down the b direction

Related literature
This research was supported by the Basic Science Research
Crystal data
Special details
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.