Fluenetil: Difference between revisions

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	\| ImageFile = Fluenetil.svg		\| ImageFile = Fluenetil.svg
	\| ImageSize = 200px		\| ImageSize = 200px
	\| ~~IUPACName~~ = 2-Fluoroethyl 4-~~biphenylylacetate~~		\| PIN = 2-Fluoroethyl (-4-yl)acetate
	\| OtherNames =		\| OtherNames = Lambrol
	\|Section1={{Chembox Identifiers		\|Section1={{Chembox Identifiers
	\| CASNo = 4301-50-2		\| CASNo = 4301-50-2
			\| CASNo_Ref = {{cascite\|correct\|CAS}}
			\| UNII_Ref = {{fdacite\|correct\|FDA}}
			\| UNII = S8K34P1L02
	\| PubChem = 20288		\| PubChem = 20288
	\| ChemSpiderID = 19113		\| ChemSpiderID = 19113
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	}}		}}

	'''Fluenetil''' (]: C<sub>16</sub>H<sub>15</sub>FO<sub>2</sub>) is a ] used in ]s.		'''Fluenetil''' (]: C<sub>16</sub>H<sub>15</sub>FO<sub>2</sub>) is a ] used in ]s.<ref>{{cite journal \|last1=Knowles \|first1=C O \|title=Chemistry and toxicology of quinoxaline, organotin, organofluorine, and formamidine acaricides. \|journal=Environmental Health Perspectives \|date=April 1976 \|volume=14 \|pages=93–102 \|doi=10.1289/ehp.761493 \|pmid=789072 \|pmc=1475104}}</ref>

	==References==		==References==
	{{reflist}}		{{reflist}}

			{{Fluoroacetates}}

	]		]
	]		]
	]		]
	]		]


	{{~~organic-compound~~-stub}}		{{ester-stub}}

Latest revision as of 18:51, 1 March 2022

Fluenetil
Names

Preferred IUPAC name 2-Fluoroethyl (-4-yl)acetate
Other names Lambrol
Identifiers
CAS Number	4301-50-2
3D model (JSmol)	Interactive image
ChemSpider	19113
ECHA InfoCard	100.149.202
PubChem CID	20288
UNII	S8K34P1L02
CompTox Dashboard (EPA)	DTXSID9058103
InChI InChI=1S/C16H15FO2/c17-10-11-19-16(18)12-13-6-8-15(9-7-13)14-4-2-1-3-5-14/h1-9H,10-12H2Key: XAERLJMOUYEBAB-UHFFFAOYSA-N InChI=1/C16H15FO2/c17-10-11-19-16(18)12-13-6-8-15(9-7-13)14-4-2-1-3-5-14/h1-9H,10-12H2Key: XAERLJMOUYEBAB-UHFFFAOYAD
SMILES O=C(OCCF)Cc1ccc(cc1)c2ccccc2
Properties
Chemical formula	C₁₆H₁₅FO₂
Molar mass	258.292 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references

Chemical compound

Fluenetil (chemical formula: C₁₆H₁₅FO₂) is a chemical compound used in acaricides.

References

Knowles, C O (April 1976). "Chemistry and toxicology of quinoxaline, organotin, organofluorine, and formamidine acaricides". Environmental Health Perspectives. 14: 93–102. doi:10.1289/ehp.761493. PMC 1475104. PMID 789072.

v t e Derivatives of fluoroacetic acid and 2-fluoroethanol
Fluoroacetate salts	Aluminum fluoroacetate Ammonium fluoroacetate Barium fluoroacetate Cadmium fluoroacetate Calcium fluoroacetate Cupric fluoroacetate Potassium fluoroacetate Sodium fluoroacetate Thallous fluoroacetate Triethyllead fluoroacetate
Fluoroacetate esters	Allyl fluoroacetate Butyl fluoroacetate Cetyl fluoroacetate Cholesteryl fluoroacetate Ethyl fluoroacetate 2-Ethylhexyl fluoroacetate Fluoroacetylcholine Fluoroaspirin Fluoroethyl fluoroacetate Isopropyl fluoroacetate Methyl fluoroacetate Methylene bis(fluoroacetate) Phenyl fluoroacetate Propyl fluoroacetate
Fluoroethyl esters	Bis(2-fluoroethyl) carbonate Bis(2-fluoroethyl) hydrogen phosphite Bis(2-fluoroethyl) phosphorofluoridate Bis(2-fluoroethyl) sulfate Bis(2-fluoroethyl) sulfite Fluenetil Fluoroethyl acetate Fluoroethyl chloroacetate Fluoroethyl chloroformate Fluoroethyl chlorosulfonate Fluoroethyl fluoroacetate Fluoroethyl nitrite Fluoroethyl trichloroacetate Tetrakis(2-fluoroethyl) orthosilicate TL-790 TL-821 Tris(2-fluoroethyl) arsenite Tris(2-fluoroethyl) borate Tris(2-fluoroethyl) phosphite Tris(2-fluoroethyl) orthoformate
Fluoroacetamides	Fluoroacetamide Fluoroacetanilide Nissol
Other	Bis(2-fluoroethyl)ether 2-chloroethyl fluorothioacetate Fluoroacetic anhydride Fluoroacetyl chloride Fluoroacetyl fluoride

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