ChemicalBook--->CAS DataBase List--->137641-05-5

137641-05-5

137641-05-5 Structure

137641-05-5 Structure
IdentificationBack Directory
[Name]

PICOLINAFEN
[CAS]

137641-05-5
[Synonyms]

PICOLINAFEN
Picolinafen [iso]
Picolinafen solution
Picolinafen Standard
picolinafen (bsi,iso)
Picolinafen Solution,100ppm
Picolinafen@100 μg/mL in Methanol
Picolinafen@1000 μg/mL in Methanol
Picolinafen?Solution in Toluene, 1000μg/mL
n-(4-fluorophenyl)-6-(α,α,α-trifluoro-m-tolyloxy)picolinamide
N-(4-FLUOROPHENYL)-6-[3-(TRIFLUOROMETHYL)PHENOXY]-2-PYRIDINECARBOXAMIDE
N-(4-FLUOROPHENYL)-6-(ALPHA,ALPHA,ALPHA-TRIFLUORO-M-TOLYLOXY)PICOLINAMIDE
2-Pyridinecarboxamide, N-(4-fluorophenyl)-6-[3-(trifluoromethyl)phenoxy]-
N-(4-Fluorophenyl)-6-(α,α,α-trifluoro-m-tolyloxy)picolinamide, N-(4-Fluorophenyl)-6-[3-(trifluoromethyl)phenoxy]-2-pyridinecarboxamide
[Molecular Formula]

C19H12F4N2O2
[MDL Number]

MFCD04040061
[MOL File]

137641-05-5.mol
[Molecular Weight]

376.3
Chemical PropertiesBack Directory
[Melting point ]

107.2-107.6°
[Boiling point ]

399.0±42.0 °C(Predicted)
[density ]

1.394±0.06 g/cm3(Predicted)
[storage temp. ]

0-6°C
[form ]

neat
[pka]

10.28±0.70(Predicted)
[Major Application]

agriculture
environmental
[InChI]

1S/C19H12F4N2O2/c20-13-7-9-14(10-8-13)24-18(26)16-5-2-6-17(25-16)27-15-4-1-3-12(11-15)19(21,22)23/h1-11H,(H,24,26)
[InChIKey]

CWKFPEBMTGKLKX-UHFFFAOYSA-N
[SMILES]

Fc1ccc(NC(=O)c2cccc(Oc3cccc(c3)C(F)(F)F)n2)cc1
[LogP]

4.367 (est)
Safety DataBack Directory
[Hazard Codes ]

N
[Risk Statements ]

50/53
[Safety Statements ]

60-61
[RIDADR ]

UN3077 9/PG 3
[WGK Germany ]

2
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Aquatic Acute 1
Aquatic Chronic 1
[Toxicity]

LD50 in rats (mg/kg): >5000 orally; >4000 dermally; LC50 in rats (mg/l): >5.9 by inhalation; LC50 in rainbow trout (96 hr): 0.281 mg/l (White)
Hazard InformationBack Directory
[Uses]

Herbicide.
[Definition]

ChEBI: Picolinafen is a pyridinecarboxamide resulting from the formal condensation of the carboxy group of 6-(m-trifluoromethylphenoxy)picolinic acid with the amino group of p-fluoroaniline. A carotenoid biosynthesis inhibitor, it is used as a herbicide for the control of broad-leaved weeds in cereal crops. It has a role as a herbicide, an agrochemical and a carotenoid biosynthesis inhibitor. It is a pyridinecarboxamide, a member of (trifluoromethyl)benzenes, an aromatic ether and a member of monofluorobenzenes.
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