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200509-41-7

200509-41-7 Structure

200509-41-7 Structure
IdentificationBack 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 PropertiesBack Directory
[Fp ]

2 °C
[storage temp. ]

2-8°C
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

Solid
[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
Safety DataBack Directory
[Symbol(GHS) ]

Flame (GHS02)Exclamation Mark (GHS07)
GHS02,GHS07
[Signal word ]

Danger
[Hazard statements ]

H225-H302-H312-H319-H332
[Precautionary statements ]

P210-P280-P305+P351+P338
[Hazard Codes ]

F,Xn
[Risk Statements ]

11-20/21/22-36
[Safety Statements ]

26-36/37-16
[RIDADR ]

UN 1648 3/PG 2
[WGK Germany ]

2
[REACH Registrations]

Inactive
[Storage Class]

3 - Flammable liquids
[Hazard Classifications]

Acute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Eye Irrit. 2
Flam. Liq. 2
Hazard InformationBack 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.
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