ChemicalBook--->CAS DataBase List--->141112-29-0

141112-29-0

141112-29-0 Structure

141112-29-0 Structure
IdentificationBack Directory
[Name]

ISOXAFLUTOLE
[CAS]

141112-29-0
[Synonyms]

MERLIN
BALANCE
Ift cpd
Hsdb 7275
Exp 31130a
Isoxautole
SOXAFLUTOLE
ISOXAFLUTOLE
Isoxaflutole 0
Isoxaflutole [iso]
Isoxaflutole 97% TC
Isoxaflutole pesticide
ISOXAFLUTOLE 45% SOLUTION
isoxaflutole (bsi, pa iso)
Isoxautole Solution,100ppm
Isoxaflutole@100 μg/mL in AcCN
Isoxaflutole 100mg [141112-29-0]
Einecs annex I index 606-054-00-7
Isoxaflutole Solution in Acetonitrile, 1000μg/mL
5-cyclopropyl-4-[2-(methylsulfonyl)-4-(trifluoromethyl)benzoyl]isoxazole
5-cyclopropyl-4-[2-methanesulfonyl-4-(trifluorome thyl)benzoyl]-1,2-oxazole
(5-Cyclopropyl-4-isoxazolyl)[2-(methylsulfonyl)-4-(trifluoromethyl)phenyl]methanone
(5-Cyclopropylisoxazol-4-yl)(2-(methylsulfonyl)-4-(trifluoromethyl)phenyl)methanone
Methanone, (5-cyclopropyl-4-isoxazolyl)[2-(methylsulfonyl)-4-(trifluoromethyl)phenyl]-
isoxaflutole (ISO) 5-cyclopropyl-1,2-oxazol-4-yl α,α,α-trifluoro-2-mesyl-p-tolyl ketone
[EINECS(EC#)]

277-704-1
[Molecular Formula]

C15H12F3NO4S
[MDL Number]

MFCD03095707
[MOL File]

141112-29-0.mol
[Molecular Weight]

359.32
Chemical PropertiesBack Directory
[Melting point ]

138-138.5° (Cain); mp 140°
[Boiling point ]

575.1±50.0 °C(Predicted)
[density ]

1.59
[Fp ]

>130 °C
[storage temp. ]

0-6°C
[solubility ]

Chloroform, DCM, Ethyl Acetate, Methanol
[form ]

neat
[pka]

-4.29±0.50(Predicted)
[color ]

White
[BRN ]

8344543
[LogP]

2.320
[CAS DataBase Reference]

141112-29-0
[EPA Substance Registry System]

Isoxaflutole (141112-29-0)
Safety DataBack Directory
[Hazard Codes ]

Xn,N
[Risk Statements ]

50/53-63
[Safety Statements ]

36/37-60-61
[RIDADR ]

UN3077 9/PG 3
[WGK Germany ]

3
[Hazardous Substances Data]

141112-29-0(Hazardous Substances Data)
[Toxicity]

LD50 in rats, quails, mallard ducks (mg/kg): >5000, >2150, >2150 orally; in rabbits (mg/kg): >2000 dermally (Luscombe)
Hazard InformationBack Directory
[Description]

Isoxaflutole is a 4-benzoyl isoxazole molecule and is used as a pre- and early post-emergence herbicide for the control of a wide range of important broadleaf and grass weeds in maize (Zea mays), both in Europe and in North America. It is also registered for use in sugarcane in Central and South America (2–4). It causes characteristic bleaching of newly developed tissues of susceptible species followed by growth cessation and necrosis. Marketed as Balance for corn (maize) in the United States, and Merlin for corn in Europe; and in sugarcane, it mixes well with metolachlor, acetochlor, dimethenamid, and atrazine to complete the weed spectrum and to reduce the application rates of the latter compounds (2). Isoxaflutole also controls triazineresistant weeds in the field (4).
[Uses]

Herbicide.
[Definition]

ChEBI:Isoxaflutole is a member of the class of isoxazoles that is 1,2-oxazole substituted by a 2-(methanesulfonyl)-4-(trifluoromethyl)benzoyl group and a cyclopropyl group at positions 4 and 5, respectively. It is a 4-hydroxyphenylpyruvate dioxygenase inhibitor which is used as a herbicide for weed control in maize and sugarcane. It has a role as an EC 1.13.11.27 (4-hydroxyphenylpyruvate dioxygenase) inhibitor, a proherbicide and an agrochemical. It is a member of cyclopropanes, a member of isoxazoles, an aromatic ketone, a member of (trifluoromethyl)benzenes and a sulfone.
[Pharmacology]

Isoxaflutole is readily taken up by roots and foliar tissues and then rapidly degraded to a diketonitrile derivative (2-cyclopropyl-3-(2-mesyl-4-trifluoromethylphenyl)- 3-oxo propanenitrile) , which is translocated throughout the plant via xylem and phloem (2,3,6,8). It is this metabolite that inhibits HPPD (7), thereby depleting the plastoquinone pools in developing leaves. Plastoquinone is a cofactor in the desaturation of phytoene, levels of which increase in bleached leaves, concomitant with decreases in colored carotenoids (6). Although bleaching is the primary symptom associated with HPPD inhibition, subsequent growth suppression and necrosis are also believed to be a consequence (8).
Isoxaflutole also degrades to the diketonitrile derivative in the soil (3,8). The half-life of isoxaflutole in soil is dependent on soil type, pH, and moisture, ranging from 12 hours to 3 days under laboratory conditions (8). The physicochemical properties of isoxaflutole and of diketonitrile play an important role in both soil and herbicidal activity and selectivity (8).
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