| 词条 | Nithiazine |
| 释义 |
| Name = | ImageFile = Nithiazine.svg | ImageAlt = | ImageCaption = | IUPACName =(E/Z)-2-Nitromethylene-1,3-thiazinane | SystematicName = | OtherNames = |Section1={{Chembox Identifiers | Abbreviations = | CASNo =58842-20-9 | CASNo_Comment = | CASNo_Ref ={{cascite|correct|??}} | CASNoOther = | ChEMBL = 2269816 | PubChem = | PubChem_Comment = | ChemSpiderID = 5013776 | ChemSpiderID_Comment =[1] | ChemSpiderID5 = | ChemSpiderIDOther = | EINECS = | EC_number = | UNNumber = | DrugBank = | KEGG = | MeSHName = | ChEBI = | RTECS = | SMILES =O=[N+](C=C1SCCCN1)[O-] | InChI =1S/C5H8N2O2S/c8-7(9)4-5-6-2-1-3-10-5/h4,6H,1-3H2/b5-4- | Beilstein = | Gmelin = | 3DMet =}} |Section2={{Chembox Properties | C=5 | H=8 | N=2 | O=2 | S=1 | Appearance =Crystals or brown powder | Density =1.388 g/cm3 | MeltingPt = | MeltingPt_notes = | BoilingPt = | BoilingPt_notes = | LogP = | VaporPressure = | HenryConstant = | AtmosphericOHRateConstant = | pKa = | pKb = | Solubility = | SolubleOther = | Solvent =}} |Section3={{Chembox Structure | CrystalStruct = | Coordination = | MolShape = }} |Section4={{Chembox Thermochemistry | DeltaHc = | DeltaHf = | Entropy = | HeatCapacity = }} |Section5={{Chembox Pharmacology | AdminRoutes = | Bioavail = | Metabolism = | HalfLife = | ProteinBound = | Excretion = | Legal_status = | Legal_US = | Legal_UK = | Legal_AU = | Legal_CA = | Pregnancy_category = | Pregnancy_AU = | Pregnancy_US = }} |Section6={{Chembox Explosive | ShockSens = | FrictionSens = | DetonationV = | REFactor = }} |Section7={{Chembox Hazards | ExternalSDS = | EUClass = | MainHazards = | NFPA-H = | NFPA-F = | NFPA-R = | NFPA-S = | RPhrases = | SPhrases = | RSPhrases = | FlashPt = | AutoignitionPt = | ExploLimits = | LD50 = | PEL = }} |Section8={{Chembox Related | OtherAnions = | OtherCations = | OtherFunction = | OtherFunction_label = | OtherCompounds = }} }}Nithiazine is a nitromethylene neonicotinoid insecticide. It is irritating to the eyes and skin, and is moderately toxic to mammals.[2] Nithiazine does not act as an acetylcholinesterase inhibitor.[3] References1. ^CSID:5013776, http://www.chemspider.com/Chemical-Structure.5013776.html (accessed 04:44, Jan 14, 2013) {{insecticides}}2. ^{{cite web | url = http://sitem.herts.ac.uk/aeru/vsdb/Reports/2155.htm | title = nithiazine (Ref: BA 32476 ) | publisher = University of Hertfordshire}} 3. ^{{cite journal| first = M. E. | last = Schroeder | first2 = R. F. | last2 = Flattum | title = The Mode of Action and Neurotoxic Properties of the Nitromethylene Heterocycle Insecticides | date = October 1984 | journal = Pesticide Biochemistry and Physiology | volume = 22 | pages = 148–160 | doi = 10.1016/0048-3575(84)90084-1 | issue = 2}} 3 : Insecticides|Nitro compounds|Neonicotinoids |
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