DIFENZOQUAT METHYLSULFATE

Base Information

• Chemical Name: DIFENZOQUAT METHYLSULFATE
• CAS No.: 43222-48-6
• Deprecated CAS: 216306-41-1,74160-38-6
• Molecular Formula: C16H17N2•CH3O4S
• Molecular Weight: 360.434
• Hs Code.: 2933199013
• European Community (EC) Number: 256-152-5
• UNII: 6Y5I03RK7C
• DSSTox Substance ID: DTXSID6024048
• Wikidata: Q1224329
• ChEMBL ID: CHEMBL1867054
• Mol file: 43222-48-6.mol

Synonyms:AVENGE;AVENGE(R);DIFENZOQUAT METHYLSULFATE;1,2-DIMETHYL-3,5-DIPHENYL-1H-PYRAZOLIUM METHYL SULFATE;1,2-dimethyl-3,5-diphenyl-1h-pyrazoliumethylsulfate;1,2-dimethyl-3,5-diphenylpyrazoliummethylsulphate;1H-Pyrazolium,1,2-dimethyl-3,5-diphenyl-,methylsulfate;1H-pyrazolium,1,2-dimethyl-3,5-diphenyl-methylsulfate

Chemical Property of DIFENZOQUAT METHYLSULFATE

Chemical Property:

• Melting Point: 146-148℃ (acetone )
• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 83.62000
• Density: g/cm³
• LogP: 3.35740
• Storage Temp.: 0-6°C
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 360.11437830
• Heavy Atom Count: 25
• Complexity: 342

Purity/Quality:

98%Min ^*data from raw suppliers

Difenzoquat methyl sulfate ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xn,N
• Statements: 22-50/53
• Safety Statements: 60-61

MSDS Files:

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Pesticides -> Herbicides, Other
• Canonical SMILES: CN1C(=CC(=[N+]1C)C2=CC=CC=C2)C3=CC=CC=C3.COS(=O)(=O)[O-]
• Uses: DIFENZOQUAT METHYLSULFATE is Herbicide; agricultural fungicide. DIFENZOQUAT METHYLSULFATE is used to control wild oats in wheat, barley, ?ax, maize, rye grass, vetches and rye grass crops. Difenzoquat Methyl Sulfate could have agricultural uses. It could help reduce downward migration of pesticides in soil/turf to allow it to better target pests.

Technology Process of DIFENZOQUAT METHYLSULFATE

There total 7 articles about DIFENZOQUAT METHYLSULFATE 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: 93.5%

1-methyl-3,5-diphenyl-1H-pyrazole (19311-79-6) → 1,2-dimethyl-3,5-diphenyl-1H-pyrazolium methyl sulphate (43222-48-6)

Guidance literature:

With sulfuric acid; In methanol; dichloromethane;

Reference yield: 91.7%

1-methyl-3,5-diphenyl-1H-pyrazole (19311-79-6) + 1,2-dichloro-ethane (107-06-2,52399-93-6) → 1,2-dimethyl-3,5-diphenyl-1H-pyrazolium methyl sulphate (43222-48-6)

Guidance literature:

With sulfuric acid; In methanol;

Reference yield: 89.1%

1,1,1-trichloroethane (71-55-6,74552-83-3) + 1-methyl-3,5-diphenyl-1H-pyrazole (19311-79-6) → 1,2-dimethyl-3,5-diphenyl-1H-pyrazolium methyl sulphate (43222-48-6)

Guidance literature:

With sulfur trioxide; In methanol;

upstream raw materials:

1-methyl-3,5-diphenyl-1H-pyrazole

dimethyl sulfate

1,2-dichloro-ethane

1,1,1-trichloroethane

Downstream raw materials:

1,2-dimethyl-3,5-diphenyl-2-pyrazolinium perchlorate

1-ethyl-3,5-diphenyl-1H-pyrazole

1-ethyl-2-methyl-3,5-diphenylpyrazolium ethyl sulfate

1-methyl-3,5-diphenyl-1H-pyrazole

Refernces

• 1、 -. "Substituted pyridinesulfonamide compound or its salt, process for preparing the same, and herbicide containing the same". . . Retrieved 2008/06/13.
• 2、 -. "5,6-Dihydro-1,2,4,6-thiatriazin-5-one-1,1-dioxides". . . Retrieved 2008/06/13.