Thiofanox: Difference between revisions

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	\| ImageFile = Thiofanox.svg		\| ImageFile = Thiofanox.svg
	\| ImageSize = 200px		\| ImageSize = 200px
	\| IUPACName = 6-(2-~~Methyl~~-2-~~propanyl)-4-oxa-8-thia~~-2,5-~~diazanon-5-en-3~~-~~one~~		\| IUPACName = N-methylcarbamate
	\| OtherNames =		\| OtherNames =
	\| Section1 = {{Chembox Identifiers		\|Section1={{Chembox Identifiers
	\| CASNo = 39196-18-4		\| CASNo = 39196-18-4
			\| CASNo_Ref = {{cascite\|correct\|CAS}}
⚫	\| PubChem = 38235
			\| UNII_Ref = {{fdacite\|correct\|FDA}}
⚫	\| ChemSpiderID = 35048
			\| UNII = 9ZE4QF28IN
	\| SMILES = O=C(ON=C(C(C)(C)C)CSC)NC
		⚫	\| PubChem = 38235
⚫	\| ~~InChI~~ = 1/C9H18N2O2S/c1-9(2,3)7(6-14-5)11-13-8(12)10-4/h6H2,1-5H3,(H,10,12)
		⚫	\| ChemSpiderID = 35048
⚫	\| ~~InChIKey~~ = FZSVSABTBYGOQH-~~UHFFFAOYAI~~
	\| ~~StdInChI~~ = 1S/C9H18N2O2S/c1-9(2,3)7(6-14-5)11-13-8(12)10-4/h6H2,1-5H3,(H,10,12)		\| SMILES = O=C(ON=C(C(C)(C)C)CSC)NC
			\| InChI = 1/C9H18N2O2S/c1-9(2,3)7(6-14-5)11-13-8(12)10-4/h6H2,1-5H3,(H,10,12)
	\| ~~StdInChIKey~~ = FZSVSABTBYGOQH-~~UHFFFAOYSA-N~~		\| InChIKey = FZSVSABTBYGOQH-UHFFFAOYAI
		⚫	\| StdInChI = 1S/C9H18N2O2S/c1-9(2,3)7(6-14-5)11-13-8(12)10-4/h6H2,1-5H3,(H,10,12)
		⚫	\| StdInChIKey = FZSVSABTBYGOQH-UHFFFAOYSA-N
	}}		}}
	\| Section2 = {{Chembox Properties		\|Section2={{Chembox Properties
	\| C=9\|H=18\|N=2\|O=2\|S=1		\| C=9 \| H=18 \| N=2 \| O=2 \| S=1
	\| Appearance =		\| Appearance =
	\| Density =		\| Density =
	\| MeltingPt =		\| MeltingPt =
	\| BoilingPt =		\| BoilingPt =
	\| Solubility =		\| Solubility =
	}}		}}
	\| Section3 = {{Chembox Hazards		\|Section3={{Chembox Hazards
	\| MainHazards =		\| MainHazards =
	\| FlashPt =		\| FlashPt =
	\| ~~Autoignition~~ =		\| AutoignitionPt =
	}}		}}
	}}		}}

	'''Thiofanox''' is a ] used in ]s and ]s.~~<ref> at www.alanwood.net.</ref>~~		'''Thiofanox''' is a ] used in ]s and ]s.

	==References==		==References==
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	==External links==		==External links==
			*{{PPDB\|638}}
	*

			{{Insecticides}}
			{{Acetylcholine metabolism and transport modulators}}

			]
	]		]
	]		]
	]		]
			]
			]


			{{organic-compound-stub}}

Latest revision as of 11:04, 7 March 2023

Thiofanox
Names

IUPAC name N-methylcarbamate
Identifiers
CAS Number	39196-18-4
3D model (JSmol)	Interactive image
ChemSpider	35048
ECHA InfoCard	100.049.388
PubChem CID	38235
UNII	9ZE4QF28IN
CompTox Dashboard (EPA)	DTXSID4042468
InChI InChI=1S/C9H18N2O2S/c1-9(2,3)7(6-14-5)11-13-8(12)10-4/h6H2,1-5H3,(H,10,12)Key: FZSVSABTBYGOQH-UHFFFAOYSA-N InChI=1/C9H18N2O2S/c1-9(2,3)7(6-14-5)11-13-8(12)10-4/h6H2,1-5H3,(H,10,12)Key: FZSVSABTBYGOQH-UHFFFAOYAI
SMILES O=C(ON=C(C(C)(C)C)CSC)NC
Properties
Chemical formula	C₉H₁₈N₂O₂S
Molar mass	218.32 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references

Chemical compound

Thiofanox is a chemical compound used in acaricides and insecticides.

References

External links

Thiofanox in the Pesticide Properties DataBase (PPDB)

v t e Pest control: Insecticides
Carbamates	Aldicarb Aminocarb Bendiocarb Butocarboxim Carbaryl Carbofuran Carbosulfan m-Cumenyl methylcarbamate Ethienocarb Fenobucarb Isoprocarb Methomyl Metolcarb Oxamyl Promecarb Propoxur
Inorganic compounds	Aluminium phosphide Boric acid Chromated copper arsenate Copper(II) arsenate Copper(I) cyanide Cryolite Diatomaceous earth Lead hydrogen arsenate Paris Green Scheele's Green
Insect growth regulators	Benzoylureas (Bistrifluron, Diflubenzuron, Flufenoxuron, Lufenuron, Noviflumuron) Hydroprene Methoprene Pyriproxyfen
Neonicotinoids	Acetamiprid Clothianidin Dinotefuran Imidacloprid Imidaclothiz Nitenpyram Nithiazine Paichongding Thiacloprid Thiamethoxam
Organochlorides	Aldrin Beta-HCH Carbon tetrachloride Chlordane Cyclodiene 1,2-DCB 1,4-DCB 1,1-DCE 1,2-DCE DDD DDE DDT DFDT Dicofol Dieldrin Endosulfan Endrin Heptachlor Kepone Lindane Methoxychlor Mirex Tetradifon Toxaphene
Organophosphorus	Acephate Azamethiphos Azinphos-methyl Bensulide Chlorethoxyfos Chlorfenvinphos Chlorpyrifos Chlorpyrifos-methyl Coumaphos Demeton-S-methyl Diazinon Dichlorvos Dicrotophos Diisopropyl fluorophosphate Dimefox Dimethoate Dioxathion Disulfoton Ethion Ethoprop Fenamiphos Fenitrothion Fenthion Fosthiazate Isoxathion Malathion Methamidophos Methidathion Mevinphos Mipafox Monocrotophos Naled Omethoate Oxydemeton-methyl Parathion Parathion-methyl Phenthoate Phorate Phosalone Phosmet Phoxim Pirimiphos-methyl Quinalphos R-16661 Schradan Temefos Tebupirimfos Terbufos Tetrachlorvinphos Tribufos Trichlorfon
Pyrethroids	Acrinathrin Allethrins Bifenthrin Bioallethrin Cyfluthrin Cyhalothrin Cypermethrin Cyphenothrin Deltamethrin Empenthrin Esfenvalerate Etofenprox Fenpropathrin Fenvalerate Flumethrin Fluvalinate Imiprothrin Metofluthrin Permethrin Phenothrin Prallethrin Pyrethrin (I, II; chrysanthemic acid) Pyrethrum Resmethrin Silafluofen Tefluthrin Tetramethrin Tralomethrin Transfluthrin
Diamides	Chlorantraniliprole Cyantraniliprole Flubendiamide
Other chemicals	Afoxolaner Amitraz Azadirachtin Bensultap Buprofezin Cartap Chlordimeform Chlorfenapyr Cyromazine Fenazaquin Fenoxycarb Fipronil Fluralaner Hydramethylnon Indoxacarb Limonene Lotilaner (+milbemycin oxime) Pyridaben Pyriprole Sarolaner Adjuvants (Piperonyl butoxide, Sesamex) Spinosad Sulfluramid Tebufenozide Tebufenpyrad Veracevine Xanthone Metaflumizone Ryanodine Ryanodol
Metabolites	Oxon Malaoxon Paraoxon TCPy
Biopesticides	Bacillus thuringiensis Baculovirus Beauveria bassiana Beauveria brongniartii Isaria fumosorosea Metarhizium acridum Metarhizium anisopliae Nomuraea rileyi Lecanicillium lecanii Paenibacillus popilliae Purpureocillium lilacinum Spinosad