ChemicalBook--->CAS DataBase List--->95977-29-0

95977-29-0

95977-29-0 Structure

95977-29-0 Structure
IdentificationBack Directory
[Name]

Haloxyfop-P
[CAS]

95977-29-0
[Synonyms]

Haloxyfop-P
Haloxyfop-p [iso]
Haloxyfop-R-methyl EC
Haloxyfop-P (free acid)
haloxyfop-P Solution, 100ppm
haloxyfop-P Solution, 1000ppm
(R)-2-[4-(3-Chloro-5-(trifluoromethyl)-2-pyridyloxy)phenoxy]propionic acid
(R)-2-[4-[[3-Chloro-5-(trifluoromethyl)-2-pyridinyl]oxy]phenoxy]propanoic acid
(R)-2-(4-((3-Chloro-5-(trifluoromethyl)pyridin-2-yl)oxy)phenoxy)propanoic acid
Propanoic acid, 2-[4-[[3-chloro-5-(trifluoromethyl)-2-pyridinyl]oxy]phenoxy]-, (2R)-
[Molecular Formula]

C15H11ClF3NO4
[MDL Number]

MFCD20036282
[MOL File]

95977-29-0.mol
[Molecular Weight]

361.7
Chemical PropertiesBack Directory
[Boiling point ]

420.3±45.0 °C(Predicted)
[density ]

1.442
[storage temp. ]

2-8°C
[solubility ]

Dichloromethane; Ethyl Acetate; Ether
[form ]

neat
[pka]

3.12±0.10(Predicted)
[color ]

White
[BRN ]

8571970
[InChI]

1S/C15H11ClF3NO4/c1-8(14(21)22)23-10-2-4-11(5-3-10)24-13-12(16)6-9(7-20-13)15(17,18)19/h2-8H,1H3,(H,21,22)/t8-/m1/s1
[InChIKey]

GOCUAJYOYBLQRH-MRVPVSSYSA-N
[SMILES]

C[C@@H](Oc1ccc(Oc2ncc(cc2Cl)C(F)(F)F)cc1)C(O)=O
[LogP]

2.800 (est)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22-52/53
[WGK Germany ]

3
[Storage Class]

6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
[Hazard Classifications]

Acute Tox. 3 Oral
Aquatic Acute 1
Aquatic Chronic 1
Hazard InformationBack Directory
[Uses]

Haloxyfop-P is a herbicide for controlling weeds in cassia fields. A pesticide residue in vegetables.
[Definition]

ChEBI: Haloxyfop-P is a 2-(4-{[3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid that has R configuration. It is the most active enantiomer of the (racemic) herbicide haloxyfop and is used (particularly as the corresponding methyl and ethoxyethyl ester proherbicides (haloxyfop-P-methyl and haloxyfop-P-etotyl, respectively) to control annual and perrenial grasses in a variety of crops. It has a role as a phenoxy herbicide, an agrochemical and an EC 6.4.1.2 (acetyl-CoA carboxylase) inhibitor. It is a conjugate acid of a haloxyfop-P(1-). It is an enantiomer of a (S)-haloxyfop.
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