Issue 0, 1983

Synthesis and X-ray crystal structure of a new potent pyrethroid acid, (±)-cis-3-[(Z)-2-chloro-3,3,3-trifluoroprop-1-enyl]-2,2-dimethylcyclopropanecarboxylic acid

Abstract

Single-crystal X-ray analysis of the title compound has established its structure and molecular geometry. Crystals are monoclinic, space group P21/c, with a= 9.487(4), b= 8.009(4), c= 16.214(6)Å, β= 119.91(1)°, Z= 4. The structure was solved by direct methods and refined by full-matrix least-squares calculations to R 0.056 over 1 242 reflections measured by diffractometer. The crystals contain centrosymmetric hydrogen-bonded dimers (O ⋯ O 2.65 Å) in which the carboxy and vinyl substituents are in a ‘bisecting’ orientation, and the C[double bond, length half m-dash]O group and one of hydrogen atoms on each methyl group point over the cyclopropane ring. The bond lengths in the ring reflect the substitution pattern.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1983, 1737-1740

Synthesis and X-ray crystal structure of a new potent pyrethroid acid, (±)-cis-3-[(Z)-2-chloro-3,3,3-trifluoroprop-1-enyl]-2,2-dimethylcyclopropanecarboxylic acid

J. F. Engel, A. T. McPhail and R. W. Miller, J. Chem. Soc., Perkin Trans. 1, 1983, 1737 DOI: 10.1039/P19830001737

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