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69806-40-2

69806-40-2 Structure

69806-40-2 Structure
IdentificationBack Directory
[Name]

Methyl 2-(4-((3-chloro-5-(trifluoromethyl)-2-pyridinyl)oxy)phenoxy)propanoate
[CAS]

69806-40-2
[Synonyms]

HALOXYFOP-METHYL
Methyl 2-(4-((3-chlo
R-(+)-haloxyfop-Methyl
Haloxyfop methyl ester
HALOXYFOP-METHYL PESTANAL, 250 MG
Haloxyfop-methyl Solution, 1000ppm
Haloxyfop-methyl @100 μg/mL in MeOH
Methyl 2-(4-((3-chloro-5-(trifluoromethyl)
Haloxyfop-methyl Solution in Methanol, 100μg/mL
METHYL-2-[4-(3-CHLORO-5-TRIFLUOROMETHYL-2-PYRIDYLOXY) PHENOXY]PROPIONATE
METHYL 2-[4-[3-CHLORO-5-(TRIFLUOROMETHYL)PYRIDIN-2-YL]OXYPHENOXY]PROPANOATE
methyl 2-(4-((3-chloro-5-(trifluoromethyl)-2-pyridinyl)oxy)phenoxy)propanoate
2-[4-(3-Chloro-5-trifluoromethylpyridin-2-yloxy)phenoxy]propanoic acid methyl ester
Propanoic acid, 2-4-3-chloro-5-(trifluoromethyl)-2-pyridinyloxyphenoxy-, methyl ester
[Molecular Formula]

C16H13ClF3NO4
[MDL Number]

MFCD01310644
[MOL File]

69806-40-2.mol
[Molecular Weight]

375.73
Chemical PropertiesBack Directory
[Melting point ]

55-57°C
[Boiling point ]

390.8±42.0 °C(Predicted)
[density ]

1.4076 (estimate)
[Fp ]

>100 °C
[storage temp. ]

0-6°C
[form ]

neat
[pka]

-1.52±0.32(Predicted)
[BRN ]

1509615
[CAS DataBase Reference]

69806-40-2
[NIST Chemistry Reference]

Haloxyfop-methyl(69806-40-2)
[EPA Substance Registry System]

Propanoic acid, 2-[4-[[3-chloro-5-(trifluoromethyl)- 2-pyridinyl]oxy]phenoxy]-, methyl ester(69806-40-2)
Safety DataBack Directory
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

22
[WGK Germany ]

3
[RTECS ]

UA2458270
[HS Code ]

29333990
Hazard InformationBack Directory
[Uses]

Haloxyfop-methyl is a herbicide used for selective post-emergence control of annual and perennial grasses in broadleaf crops.
[Definition]

ChEBI:Methyl 2-(4-{[3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoate is the methyl ester of 2-(4-{[3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid. It is a methyl ester, an aromatic ether, an organochlorine compound, an organofluorine compound and a member of pyridines. It is functionally related to a 2-(4-{[3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid.
[Metabolic pathway]

In all soils tested, 14C-haloxyprop methyl is rapidly hydrolyzed to the corresponding haloxyprop acid, providing there is moisture in excess of the wilting point. In air-dried soils, little hydrolysis of haloxypropm ethyl to acid occurs. In moist sterile soils, there is a loss of solvent extractable radioactivity with time. These losses follow first-order kinetics, with half- lives of 27, 38, and 92 days respectively in the sandy loam, heavy clay, and clay loam soil types.
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