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Thiacloprid

Names
IUPAC name {(2Z)-3--1,3-thiazolidin-2-ylidene}cyanamide
Other names -2-thiazolidinylidene]cyanamide
Identifiers
CAS Number	111988-49​-9
3D model (JSmol)	Interactive image
ChEBI	CHEBI:39176
ChemSpider	103099
DrugBank	DB08620
ECHA InfoCard	100.129.728
KEGG	C18512
PubChem CID	115224
UNII	DSV3A944A4
CompTox Dashboard (EPA)	DTXSID7034961
InChI InChI=1S/C10H9ClN4S/c11-9-2-1-8(5-13-9)6-15-3-4-16-10(15)14-7-12/h1-2,5H,3-4,6H2/b14-10-Key: HOKKPVIRMVDYPB-UVTDQMKNSA-N
SMILES Clc1ncc(cc1)CN2C(=N\C#N)\SCC2
Properties
Chemical formula	C10H9ClN4S
Molar mass	252.72 g·mol
Appearance	Yellowish crystalline solid
Density	1.46 g at 20 °C
Melting point	136 °C (277 °F; 409 K)
Solubility in water	185 mg/L at 20°C
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is  ?) Infobox references

Thiacloprid is an insecticide of the neonicotinoid class. Its mechanism of action involves disruption of the insect's nervous system by inhibiting nicotinic acetylcholine receptors. Thiacloprid was developed by Bayer CropScience for use on agricultural crops to control of a variety of sucking and chewing insects, primarily aphids and whiteflies.

References

1. "Thiacloprid". Bayer CropScience Crop Compendium. Bayer CropScience. Retrieved 30 November 2011.
2. ^ Thiacloprid Pesticide Fact Sheet, United States Environmental Protection Agency
3. Schuld, Michael; Schmuck, Richard (2000). Ecotoxicology. 9 (3): 197. doi:10.1023/A:1008994705074. {{cite journal}}: Missing or empty |title= (help)

• Insecticides
• Thiazolidines
• Pyridines
• Organochlorides
• Nitriles