ETHIOFENCARB-SULFONE

Base Information

• Chemical Name: ETHIOFENCARB-SULFONE
• CAS No.: 53380-23-7
• Molecular Formula: C11H15NO4S
• Molecular Weight: 257.31
• European Community (EC) Number: 634-875-0
• DSSTox Substance ID: DTXSID80968033
• Nikkaji Number: J531.099G
• Wikidata: Q82950714
• Metabolomics Workbench ID: 48970
• Mol file: 53380-23-7.mol

Synonyms:Ethiofencarb-sulfone;53380-23-7;Croneton sulfone;Ethiofencarb sulfone;Phenol, 2-((ethylsulfonyl)methyl)-, methylcarbamate;[2-(ethylsulfonylmethyl)phenyl] N-methylcarbamate;2-((Ethylsulfonyl)methyl)phenol methylcarbamate;BRN 1988595;2-(Ethylsulfonylmethyl)phenyl methylcarbamate;ethiofencarbsulfone;SCHEMBL22498740;DTXSID80968033;CHEBI:174373;1ST20263;LS-104655;[2-(ethylsulonylmethyl)phenyl] N-methylcarbamate;2-[(ethanesulfonyl)methyl]phenyl N-methylcarbamate;Ethiofencarb-sulfone, PESTANAL(R), analytical standard;Phenol, 2-[(ethylsulfonyl)methyl]-, 1-(N-methylcarbamate);2-[(Ethanesulfonyl)methyl]phenyl hydrogen methylcarbonimidate

Chemical Property of ETHIOFENCARB-SULFONE

Chemical Property:

• Vapor Pressure: 2.86E-08mmHg at 25°C
• Boiling Point: 449.4°Cat760mmHg
• PKA: 11.96±0.46(Predicted)
• Flash Point: 225.6°C
• Density: 1.247g/cm³
• Storage Temp.: APPROX 4°C
• XLogP3: 0.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 257.07217913
• Heavy Atom Count: 17
• Complexity: 347

Purity/Quality:

98%Min ^*data from raw suppliers

Ethiofencarb Sulfone ^*data from reagent suppliers

Safty Information:

• Pictogram(s): 1988595
• Hazard Codes: Xn
• Statements: 22

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCS(=O)(=O)CC1=CC=CC=C1OC(=O)NC
• Uses: Ethiofencarb Sulfone is a metabolite of Croneton, a carbamate insecticide.

Technology Process of ETHIOFENCARB-SULFONE

There total 2 articles about ETHIOFENCARB-SULFONE 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:

ethiofencarb (29973-13-5) → ethiofencarb sulfone (53380-23-7)

Guidance literature:

With dihydrogen peroxide; tungsten(VI) oxide;

DOI:10.1002/ps.2780430409

Reference yield:

→ ethiofencarb sulfone (53380-23-7)

Guidance literature:

Aus /BRN= 49515/ + CH3-NCO;

Reference yield:

ethiofencarb sulfone (53380-23-7) → 2-ethylsulfonylmethylphenol (53380-27-1)

Guidance literature:

With potassium hydroxide; In methanol;

DOI:10.1002/ps.2780430409

upstream raw materials:

ethiofencarb

Downstream raw materials:

2-ethylsulfonylmethylphenol

Refernces