Draft:Cycloxaprid

Cycloxaprid
Names
IUPAC name
(1S,8R)-5-[(6-chloropyridin-3-yl)methyl]-7-nitro-11-oxa-2,5-diazatricyclo[6.2.1.02,6]undec-6-ene
Other names
Cycloxaprid, 5,8-Epoxy-1H-imidazo[1,2-a]azepine, 1-[(6-chloro-3-pyridinyl)methyl]-2,3,5,6,7,8-hexahydro-9-nitro-, (5S,8R)-
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
  • InChI=1S/C14H15ClN4O3/c15-11-3-1-9(7-16-11)8-17-5-6-18-12-4-2-10(22-12)13(14(17)18)19(20)21/h1,3,7,10,12H,2,4-6,8H2/t10-,12+/m1/s1
    Key: NDHXMRFNYMNBKO-PWSUYJOCSA-N
  • C1C[C@H]2N3CCN(C3=C([C@@H]1O2)[N+](=O)[O-])CC4=CN=C(C=C4)Cl
Properties
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Molar mass 322.75 g/mol
Hazards
GHS labelling:
GHS07: Exclamation mark GHS08: Health hazard GHS09: Environmental hazard
Warning
H302, H312, H315, H319, H332, H351, H410
Preview warning: Omit Rules: keep H410, omit H400
P273, P280, P301+P312, P305+P351+P338, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Cycloxaprid is a neonicotinoid insecticide derived from the (nitromethylene)imidazole (NMI) analogue of imidacloprid. First reported in 2008[1], it is a novel insecticide developed to control pests that have developed resistance to imidacloprid, particularly targeting lepidopteran pests and whiteflies in rice cultivation. Currently, limited information is available regarding its environmental impact, ecotoxicology, or effects on human health.[2]

  1. ^ Shao, Xusheng; Zhang, Wenwen; Peng, Yanqing; Li, Zhong; Tian, Zhongzhen; Qian, Xuhong (2008-12-15). "cis-Nitromethylene neonicotinoids as new nicotinic family: Synthesis, structural diversity, and insecticidal evaluation of hexahydroimidazo[1,2-α]pyridine". Bioorganic & Medicinal Chemistry Letters. 18 (24): 6513–6516. doi:10.1016/j.bmcl.2008.10.048. ISSN 0960-894X. PMID 18951786.
  2. ^ Hertfordshire, University of. "Cycloxaprid". sitem.herts.ac.uk. Retrieved 2024-11-09.