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Isoxaflutole

Base Information Edit
  • Chemical Name:Isoxaflutole
  • CAS No.:141112-29-0
  • Molecular Formula:C15H12F3NO4S
  • Molecular Weight:359.326
  • Hs Code.:
  • European Community (EC) Number:604-222-4
  • UNII:0T9R0O0EYT
  • DSSTox Substance ID:DTXSID5034723
  • Nikkaji Number:J794.343A
  • Wikidata:Q15632908
  • Metabolomics Workbench ID:153825
  • ChEMBL ID:CHEMBL1887147
  • Mol file:141112-29-0.mol
Isoxaflutole

Synonyms:IFT cpd;isoxaflutole

Suppliers and Price of Isoxaflutole
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • Isoxaflutole
  • 10mg
  • $ 580.00
  • Sigma-Aldrich
  • Isoxaflutole PESTANAL?, analytical standard
  • 100mg
  • $ 119.00
  • Medical Isotopes, Inc.
  • Isoxaflutole
  • 2.5 mg
  • $ 675.00
  • Crysdot
  • (5-Cyclopropylisoxazol-4-yl)(2-(methylsulfonyl)-4-(trifluoromethyl)phenyl)methanone 95+%
  • 10g
  • $ 475.00
  • Crysdot
  • (5-Cyclopropylisoxazol-4-yl)(2-(methylsulfonyl)-4-(trifluoromethyl)phenyl)methanone 95+%
  • 1g
  • $ 89.00
  • Crysdot
  • (5-Cyclopropylisoxazol-4-yl)(2-(methylsulfonyl)-4-(trifluoromethyl)phenyl)methanone 95+%
  • 5g
  • $ 297.00
  • Chemenu
  • (5-cyclopropylisoxazol-4-yl)(2-(methylsulfonyl)-4-(trifluoromethyl)phenyl)methanone 95%
  • 5g
  • $ 281.00
  • Chemenu
  • (5-cyclopropylisoxazol-4-yl)(2-(methylsulfonyl)-4-(trifluoromethyl)phenyl)methanone 95%
  • 10g
  • $ 449.00
  • American Custom Chemicals Corporation
  • ISOXAFLUTOLE 95.00%
  • 5MG
  • $ 496.00
Total 69 raw suppliers
Chemical Property of Isoxaflutole Edit
Chemical Property:
  • Vapor Pressure:3.15E-13mmHg at 25°C 
  • Melting Point:138-138.5° (Cain); mp 140° 
  • Refractive Index:1.534 
  • Boiling Point:575.1 °C at 760 mmHg 
  • PKA:-4.29±0.50(Predicted) 
  • Flash Point:301.6 °C 
  • PSA:85.62000 
  • Density:1.455 g/cm3 
  • LogP:4.28610 
  • Storage Temp.:0-6°C 
  • Solubility.:Chloroform, DCM, Ethyl Acetate, Methanol 
  • XLogP3:2.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:8
  • Rotatable Bond Count:4
  • Exact Mass:359.04391352
  • Heavy Atom Count:24
  • Complexity:597
Purity/Quality:

99.9% *data from raw suppliers

Isoxaflutole *data from reagent suppliers

Safty Information:
  • Pictogram(s): HarmfulXn,Dangerous
  • Hazard Codes:Xn,N 
  • Statements: 50/53-63 
  • Safety Statements: 36/37-60-61 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Chemical Classes:Pesticides -> Herbicides, Other
  • Canonical SMILES:CS(=O)(=O)C1=C(C=CC(=C1)C(F)(F)F)C(=O)C2=C(ON=C2)C3CC3
  • Recent ClinicalTrials:Safety and Efficacy of Merlin (Ethanol and Glycolic Acid Mixture) for Episodic Treatment of Cold Sores
  • 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. Isoxaflutole is an pesticide used to selectively control both grass and broad-leaved weeds in maize and sugar cane. Isoxaflutole is known to work by inhibiting the enzyme 4-Hydroxyphenylpyruvate dioxygenase (HPPD) which results in the disruption of pigment biosynthesis.
Technology Process of Isoxaflutole

There total 11 articles about Isoxaflutole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 97.7%

Guidance literature:
With hydroxylamine hydrochloride; water; In methanol; at 30 - 50 ℃; for 3.5h;

Reference yield: 96.7%

Guidance literature:
With hydroxylamine hydrochloride; In ethanol; water; at 20 ℃; for 5h;

Reference yield: 92.0%

Guidance literature:
With hydroxylamine hydrochloride; In ethanol; for 3h; Large scale;
Refernces Edit
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