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Formetanate: Difference between revisions

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| ImageFile = Formetanate.svg | ImageFile = Formetanate.svg
| ImageSize = 200px | ImageSize = 200px
| IUPACName = 3-{(''E'')-amino}phenyl methylcarbamate | IUPACName = 3-<nowiki/>{(''E'')-amino}phenyl methylcarbamate
| OtherNames = Carzol | OtherNames = Carzol
| Section1 = {{Chembox Identifiers |Section1={{Chembox Identifiers
| CASNo = 22259-30-9 | CASNo = 22259-30-9
| CASNo_Ref = {{cascite|correct|}} | CASNo_Ref = {{cascite|correct|}}
| CASNo1 = 23422-53-9 | CASNo1 = 23422-53-9
| CASNo1_Ref = {{cascite|correct|}} | CASNo1_Ref = {{cascite|correct|}}
| CASNo1_Comment = (]) | CASNo1_Comment = (])
| UNII_Ref = {{fdacite|correct|FDA}}
| PubChem = 31099
| UNII = 532HEC1KKM
| ChemSpiderID = 28856
| UNII1_Ref = {{fdacite|correct|FDA}}
| SMILES = O=C(Oc1cccc(\N=C\N(C)C)c1)NC
| UNII1 = W0Y3OP0N2Z
| InChI = 1/C11H15N3O2/c1-12-11(15)16-10-6-4-5-9(7-10)13-8-14(2)3/h4-8H,1-3H3,(H,12,15)/b13-8+
| UNII1_Comment = (])
| InChIKey = RMFNNCGOSPBBAD-MDWZMJQEBJ
| PubChem = 31099
| StdInChI = 1S/C11H15N3O2/c1-12-11(15)16-10-6-4-5-9(7-10)13-8-14(2)3/h4-8H,1-3H3,(H,12,15)/b13-8+
| ChemSpiderID = 28856
| StdInChIKey = RMFNNCGOSPBBAD-MDWZMJQESA-N
| SMILES = O=C(Oc1cccc(\N=C\N(C)C)c1)NC
| InChI = 1/C11H15N3O2/c1-12-11(15)16-10-6-4-5-9(7-10)13-8-14(2)3/h4-8H,1-3H3,(H,12,15)/b13-8+
| InChIKey = RMFNNCGOSPBBAD-MDWZMJQEBJ
| StdInChI = 1S/C11H15N3O2/c1-12-11(15)16-10-6-4-5-9(7-10)13-8-14(2)3/h4-8H,1-3H3,(H,12,15)/b13-8+
| StdInChIKey = RMFNNCGOSPBBAD-MDWZMJQESA-N
}} }}
| Section2 = {{Chembox Properties |Section2={{Chembox Properties
| C=11|H=15|N=3|O=2 | C=11 | H=15 | N=3 | O=2
| Appearance = | Appearance =
| Density = | Density =
| MeltingPt = | MeltingPt = 102 °C
| BoilingPt = | BoilingPt =
| Solubility = | Solubility =
}} }}
| Section3 = {{Chembox Hazards |Section3={{Chembox Hazards
| MainHazards = | MainHazards =
| FlashPt = | FlashPt =
| Autoignition = | AutoignitionPt =
}} }}
}} }}


'''Formetanate''' is an ] and ].<ref>, alanwood.net</ref> It is used on ] grown for seed and on some fruits, including ], ], and ]s.<ref>, Pesticide Management Education Program</ref> '''Formetanate''' is an ] and ]. It is used on ] grown for seed and on some fruits, including ], ], and ]s.<ref>, Pesticide Management Education Program</ref>


==See also== ==See also==
* ] * ]

==External links==
*


==References== ==References==
{{Reflist}} {{Reflist}}


==External links==
{{Cholinergics}}
* {{PPDB|360}}


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

]
] ]
] ]
] ]
]



{{organic-compound-stub}} {{organic-compound-stub}}

Latest revision as of 13:24, 21 March 2024

Formetanate
Names
IUPAC name 3-{(E)-amino}phenyl methylcarbamate
Other names Carzol
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.040.784 Edit this at Wikidata
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C11H15N3O2/c1-12-11(15)16-10-6-4-5-9(7-10)13-8-14(2)3/h4-8H,1-3H3,(H,12,15)/b13-8+Key: RMFNNCGOSPBBAD-MDWZMJQESA-N
  • InChI=1/C11H15N3O2/c1-12-11(15)16-10-6-4-5-9(7-10)13-8-14(2)3/h4-8H,1-3H3,(H,12,15)/b13-8+Key: RMFNNCGOSPBBAD-MDWZMJQEBJ
SMILES
  • O=C(Oc1cccc(\N=C\N(C)C)c1)NC
Properties
Chemical formula C11H15N3O2
Molar mass 221.260 g·mol
Melting point 102 °C
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

Formetanate is an insecticide and acaricide. It is used on alfalfa grown for seed and on some fruits, including citrus, pome, and stone fruits.

See also

References

  1. Formetanate HCL (Carzol) Chemical Fact Sheet, Pesticide Management Education Program

External links

  • Formetanate in the Pesticide Properties DataBase (PPDB)
Pest control: Insecticides
Carbamates
Inorganic compounds
Insect growth regulators
Neonicotinoids
Organochlorides
Organophosphorus
Pyrethroids
Diamides
Other chemicals
Metabolites
Biopesticides
Acetylcholine metabolism and transport modulators
Enzyme
(modulators)
ChATTooltip Choline acetyltransferase
AChETooltip Acetylcholinesterase
BChETooltip Butyrylcholinesterase
Transporter
(modulators)
CHTTooltip Choline transporter
VAChTTooltip Vesicular acetylcholine transporter
Release
(modulators)
Inhibitors
Enhancers
See also
Receptor/signaling modulators
Muscarinic acetylcholine receptor modulators
Nicotinic acetylcholine receptor modulators
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