Misplaced Pages

Fluenetil: Difference between revisions

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Browse history interactively← Previous editContent deleted Content addedVisualWikitext
Revision as of 15:22, 26 June 2012 editEdgar181 (talk | contribs)Extended confirmed users196,325 edits chembox and data added; categories← Previous edit Latest revision as of 18:51, 1 March 2022 edit undoSaralicia (talk | contribs)Extended confirmed users22,226 editsNo edit summary 
(13 intermediate revisions by 10 users not shown)
Line 2: Line 2:
| 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}}
| PubChem = 20288
| UNII_Ref = {{fdacite|correct|FDA}}
| ChemSpiderID = 19113
| UNII = S8K34P1L02
| SMILES = O=C(OCCF)Cc1ccc(cc1)c2ccccc2
| PubChem = 20288
| 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,10-12H2
| ChemSpiderID = 19113
| InChIKey = XAERLJMOUYEBAB-UHFFFAOYAD
| SMILES = O=C(OCCF)Cc1ccc(cc1)c2ccccc2
| StdInChI = 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,10-12H2
| 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,10-12H2
| StdInChIKey = XAERLJMOUYEBAB-UHFFFAOYSA-N
| InChIKey = XAERLJMOUYEBAB-UHFFFAOYAD
| StdInChI = 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,10-12H2
| StdInChIKey = XAERLJMOUYEBAB-UHFFFAOYSA-N
}} }}
| Section2 = {{Chembox Properties |Section2={{Chembox Properties
| C=16|H=15|F=1|O=2 | C=16 | H=15 | F=1 | O=2
| Appearance = | Appearance =
| Density = | Density =
| MeltingPt = | MeltingPt =
| BoilingPt = | BoilingPt =
| Solubility = | Solubility =
}} }}
| Section3 = {{Chembox Hazards |Section3={{Chembox Hazards
| MainHazards = | MainHazards =
| FlashPt = | FlashPt =
| Autoignition = | AutoignitionPt =
}} }}
}} }}


'''Fluenetil''' (]: C<sub>16</sub>H<sub>15</sub>FO<sub>2</sub>) is a ] used in ]s.<ref></ref> '''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}}
]

]
]
]
]


{{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
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.149.202 Edit this at Wikidata
PubChem CID
UNII
CompTox Dashboard (EPA)
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

  1. 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.
Derivatives of fluoroacetic acid and 2-fluoroethanol
Fluoroacetate salts
Fluoroacetate esters
Fluoroethyl esters
Fluoroacetamides
Other


Stub icon

This article about an ester is a stub. You can help Misplaced Pages by expanding it.

Categories: