Ethametsulfuron-methyl

Base Information

• Chemical Name: Ethametsulfuron-methyl
• CAS No.: 97780-06-8
• Molecular Formula: C15H18N6O6S
• Molecular Weight: 410.411
• European Community (EC) Number: 619-290-0
• UNII: C54ZP2XRYX
• DSSTox Substance ID: DTXSID9034573
• Nikkaji Number: J367.438J
• Wikidata: Q27275205
• ChEMBL ID: CHEMBL1885280
• Mol file: 97780-06-8.mol

Synonyms:ethametsulfuron-methyl;methyl 2-(((((4-ethoxy-6-(methylamino)-1,3,5-triazin-2-yl)amino)carbonyl)amino)sulfonyl)benzoate

Chemical Property of Ethametsulfuron-methyl

Chemical Property:

• Appearance/Colour: Light tan Solid
• Vapor Pressure: 0-0Pa at 25-45.3℃
• Melting Point: 192-194 °C
• Refractive Index: 1.606
• Boiling Point: 316.8℃
• PKA: 2.54±0.10(Predicted)
• PSA: 169.88000
• Density: 1.473 g/cm³
• LogP: 2.22670
• Storage Temp.: 0-6°C
• Solubility.: DMSO (Slightly, Sonicated), Methanol (Slightly, Heated, Sonicated)
• XLogP3: 1.8
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 10
• Rotatable Bond Count: 8
• Exact Mass: 410.10085349
• Heavy Atom Count: 28
• Complexity: 641

Purity/Quality:

99.9% ^*data from raw suppliers

Ethametsulfuron-methyl ^*data from reagent suppliers

Safty Information:

• Pictogram(s): N
• Hazard Codes: N
• Statements: 50/53
• Safety Statements: 60-61

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCOC1=NC(=NC(=N1)NC(=O)NS(=O)(=O)C2=CC=CC=C2C(=O)OC)NC
• Uses: Ethametsulfuron-methyl is a regulator of the early steps of complement activation on mucosal surfaces. It can be used in combination treatment of ohmic heating with various essential oil components for inactivation of food-?borne pathogens in buffered peptone water and salsa.

Technology Process of Ethametsulfuron-methyl

There total 2 articles about Ethametsulfuron-methyl 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:

2-(methoxycarbonyl)benzenesulfonyl isocyanate (74222-95-0) + 6-ethoxy-N-methyl-[1,3,5]triazine-2,4-diamine (62096-63-3) → 2-[[(4-ethoxy-6-methylamino-1,3,5-triazin-2-yl)aminocarbonyl]aminosulfonyl]benzoic acid,methyl ester (97780-06-8)

Guidance literature:

In dichloromethane;

Reference yield:

→ 2-[[(4-ethoxy-6-methylamino-1,3,5-triazin-2-yl)aminocarbonyl]aminosulfonyl]benzoic acid,methyl ester (97780-06-8)

Guidance literature:

upstream raw materials:

2-(methoxycarbonyl)benzenesulfonyl isocyanate

6-ethoxy-N-methyl-[1,3,5]triazine-2,4-diamine

Refernces

• 1、 -. "N-phenylpyrrolidines". . . Retrieved 2008/06/13.