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Chemical Structure| 74223-64-6 Chemical Structure| 74223-64-6
Chemical Structure| 74223-64-6

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Metsulfuron-methyl is a sulfonylurea herbicide widely used to control broadleaf weeds and annual grasses in rice, maize, wheat, and barley.

Synonyms: Metsulfuron-methyl

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Product Details of Metsulfuron-methyl

CAS No. :74223-64-6
Formula : C14H15N5O6S
M.W : 381.36
SMILES Code : S(=O)(=O)(NC(=O)NC1(=NC(OC)=NC(=N1)C))C2(=C(C(=O)OC)C=CC=C2)
Synonyms :
Metsulfuron-methyl
MDL No. :MFCD00128061
InChI Key :RSMUVYRMZCOLBH-UHFFFAOYSA-N
Pubchem ID :52999

Safety of Metsulfuron-methyl

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H361-H372-H410
Precautionary Statements:P201-P264-P280-P301+P330+P331-P312
Class:9
UN#:3077
Packing Group:

Application In Synthesis of Metsulfuron-methyl

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 74223-64-6 ]

[ 74223-64-6 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 74223-64-6 ]
  • [ 93-58-3 ]
  • [ 57683-71-3 ]
  • [ 74222-95-0 ]
  • [ 1668-54-8 ]
  • 2-Isocyanato-4-methoxy-6-methyl-[1,3,5]triazine [ No CAS ]
  • [ 18712-14-6 ]
  • 2
  • [ 74223-64-6 ]
  • [ 1668-54-8 ]
  • (o-Methoxycarbonylphenylsulfonyl)carbamic acid [ No CAS ]
  • 3
  • [ 74223-64-6 ]
  • [ 57683-71-3 ]
  • [ 1668-54-8 ]
  • methyl 2-[[[[(4-hydroxy-6-methyl-1,3,5-triazine-2-yl)amino]carbonyl]amino]sulfonyl]benzoate [ No CAS ]
  • methyl 2-[[[[[[[(acetylamino)carbonyl]amino]carbonyl]amino]carbonyl]amino]sulfonyl]benzoate [ No CAS ]
  • 4
  • [ 1668-54-8 ]
  • [ 26638-43-7 ]
  • [ 74223-64-6 ]
YieldReaction ConditionsOperation in experiment
55% In 1-methyl-pyrrolidin-2-one; EXAMPLE 3 Preparation of 2-[[(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]aminosulfonyl]benzoic acid, methyl ester A slurry of 10.0 grams (0.042 moles) of 2-carbomethoxybenzenesulfonyl chloride, 5.0 grams (0.0357 moles) 4-methoxy-6-methyl-1,3,5-triazin-2-amine and 6.0 grams (0.092 moles) sodium cyanate in 60 ml N-methylpyrrolidinone was stirred 2 hours at 80° C. The reaction was cooled to 25° C., diluted with 200 ml saturated sodium bicarbonate solution, and filtered. The filtrate was acidified with dilute hydrochloric acid and the product was collected by filtration and dried to give the title compound in 55percent yield. The IR spectrum of the title compound was identical to that of an authentic sample prepared as taught in U.S. Pat. No. 4,383,113.
  • 5
  • [ 74222-95-0 ]
  • [ 1668-54-8 ]
  • [ 74223-64-6 ]
YieldReaction ConditionsOperation in experiment
In dichloromethane; EXAMPLE 12 N-[(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-2- methoxycarbonylbenzenesulfonamide To an anhydrous suspension of 1.4 g of <strong>[1668-54-8]2-amino-4-methoxy-6-methyl-1,3,5-triazine</strong> in 25 ml of methylene chloride was added with stirring at ambient temperature and pressure 2.4 g of 2-methoxycarbonylbenzenesulfonyl isocyanate. The mixture was thereafter stirred for 16 hours and filtered. The filtrate was evaporated to dryness, the residue was triturated with butyl chloride and the product removed by filtration. The product thus obtained melted at 165°, and had absorption peaks in the infrared at 1550, 1600, 1680 and 1700 cm-1 and in the NMR spectrum at 2.5, 3.65, 4.0 with an aromatic multiplet at 7.2-8 ppm.
In dichloromethane; at 20℃; for 16h; Example 1: Preparation of Amorphous Metsulfuron-Methyl in Accordance with the Disclosure of EP 0318276 A1 (0062) To an anhydrous suspension of 1.4 g of <strong>[1668-54-8]2-amino-4-methoxy-6-methyl-1,3,5-triazine</strong> in 25 ml of methylene chloride is added with stirring at ambient temperature and pressure 2.4 g of 2-methoxycarbonylbenzenesulfonylisocyanate. The mixture is thereafter stirred for 16 hours and filtered. The filtrate is evaporated to dryness, the residue is triturated with butyl chloride and the product removed by filtration.
  • 6
  • [ 74223-64-6 ]
  • [ 57683-71-3 ]
  • C13H15N5O7S [ No CAS ]
  • [ 1668-54-8 ]
  • N-(carbomethoxy phenylsulfonyl)-N'-methyl urea [ No CAS ]
  • methyl 2-[[[[(4-hydroxy-6-methyl-1,3,5-triazine-2-yl)amino]carbonyl]amino]sulfonyl]benzoate [ No CAS ]
  • methyl 2-[[[[[[[(acetylamino)carbonyl]amino]carbonyl]amino]carbonyl]amino]sulfonyl]benzoate [ No CAS ]
 

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