| Identification | Back Directory | [Name]
Quizalofop-p-tefuryl solution | [CAS]
200509-41-7 | [Synonyms]
Quizalofop-p-tefuryl solution
(2R)-(Tetrahydrofuran-2-yl)methyl 2-(4-((6-chloroquinoxalin-2-yl)oxy)phenoxy)propanoate
Propanoic acid, 2-[4-[(6-chloro-2-quinoxalinyl)oxy]phenoxy]-, (tetrahydro-2-furanyl)methyl ester, (2R)- | [EINECS(EC#)]
682-785-5 | [Molecular Formula]
C22H21ClN2O5 | [MOL File]
200509-41-7.mol | [Molecular Weight]
428.87 |
| Chemical Properties | Back Directory | [Boiling point ]
579.599±50.00 °C(Press: 760.00 Torr)(predicted) | [density ]
1.317±0.06 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted) | [Fp ]
2 °C | [storage temp. ]
2-8°C | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
Solid | [pka]
-1.25 | [color ]
Pale Yellow to Yellow | [Major Application]
agriculture | [InChI]
1S/C22H21ClN2O5/c1-14(22(26)28-13-18-3-2-10-27-18)29-16-5-7-17(8-6-16)30-21-12-24-20-11-15(23)4-9-19(20)25-21/h4-9,11-12,14,18H,2-3,10,13H2,1H3/t14-,18?/m1/s1 | [InChIKey]
BBKDWPHJZANJGB-IKJXHCRLSA-N | [SMILES]
C[C@@H](Oc1ccc(Oc2cnc3cc(Cl)ccc3n2)cc1)C(=O)OCC4CCCO4 |
| Hazard Information | Back Directory | [Uses]
Quizalofop-P-tefuryl has been used as an analytical reference standard for the quantification of the analyte in soil samples using ultra high- performance liquid chromatography coupled to orbitrap mass spectrometry (UHPLC-Orbitrap-MS).', 'Refer to the productμs Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support. | [Definition]
ChEBI: Quizalofop-P-tefuryl is a tetrahydrofurylmethyl ester resulting from the formyl condensation of the carboxy group of quizalofop-P with the hydroxy group of tetrahydrofurfuryl alcohol. It has a role as a proherbicide and an agrochemical. It is a quinoxaline herbicide, a tetrahydrofurylmethyl ester, an aromatic ether and an organochlorine compound. It is functionally related to a quizalofop-P and a tetrahydrofurfuryl alcohol. | [Production Methods]
Quizalofop-P-tefuryl is commercially produced through a chiral transesterification process where the ethyl ester intermediate (R)-2-[4-(6-chloroquinoxalin-2-yloxy)phenoxy]propionate, synthesised via etherification of 2,6-dichloroquinoxaline with hydroquinone followed by stereoselective alkylation with an (S)-2-halopropionate, is reacted with tetrahydrofurfuryl alcohol in the presence of dibutyltin oxide catalyst, yielding the active compound. | [Mechanism of action]
Systemic, absorbed through leaves and translocated. Acetyl CoA carboxylase inhibitor (ACCase) - distrupts fatty acid biosynthesis and lipid formation. | [Pesticide Type]
Herbicide |
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| Company Name: |
Energy Chemical
|
| Telephone: |
021-58432009 400-005-6266 |
| Website: |
http://www.energy-chemical.com |
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