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Phenmedipham-ethyl

Base Information
  • Chemical Name:Phenmedipham-ethyl
  • CAS No.:13684-44-1
  • Molecular Formula:C17H18N2O4
  • Molecular Weight:314.339
  • Hs Code.:2924299090
  • European Community (EC) Number:802-885-6
  • UNII:Z56KWX34F9
  • DSSTox Substance ID:DTXSID2075009
  • Nikkaji Number:J22.314J
  • Wikidata:Q27295013
  • Mol file:13684-44-1.mol
Phenmedipham-ethyl

Synonyms:Phenmedipham-ethyl;13684-44-1;Phenmedipham-ethyl [ISO];(3-Methylphenyl)carbamic acid 3-[(ethoxycarbonyl)amino]phenyl ester;Ethyl (3-((m-tolylcarbamoyl)oxy)phenyl)carbamate;Z56KWX34F9;[3-(ethoxycarbonylamino)phenyl] N-(3-methylphenyl)carbamate;Carbamic acid, (3-methylphenyl)-, 3-((ethoxycarbonyl)amino)phenyl ester;Phenmedipham ethyl;UNII-Z56KWX34F9;(3-methylphenyl)carbamic acid 3-((ethoxycarbonyl)amino)phenyl ester;3-((ETHOXYCARBONYL)AMINO)PHENYL N-(3-METHYLPHENYL)CARBAMATE;3-[(ETHOXYCARBONYL)AMINO]PHENYL N-(3-METHYLPHENYL)CARBAMATE;ethyl 3-(3-methylcarbaniloyloxy)carbanilate;SCHEMBL134424;3-Ethoxycarbonylaminophenyl N-3-methylphenylcarbamate;DTXSID2075009;AMY7522;BCP33325;MFCD13194954;BS-53170;CS-0151528;Phenmedipham-ethyl 100 microg/mL in Acetone;Ethyl(3-((m-tolylcarbamoyl)oxy)phenyl)carbamate;Phenmedipham-ethyl, PESTANAL(R), analytical standard;Q27295013;ETHYL N-(3-(N-(3-METHYLPHENYL)CARBAMOYLOXY)PHENYL)CARBAMATE;CARBANILIC ACID, M-METHYL-, ESTER WITH ETHYL M-HYDROXYCARBANILATE;ETHYL N-(3-(N'-(3'-METHYLPHENYL)CARBAMOYLOXY)PHENYL)CARBAMATE;CARBAMIC ACID, N-(3-METHYLPHENYL)-, 3-((ETHOXYCARBONYL)AMINO)PHENYL ESTER;CARBANILIC ACID, M-HYDROXY-, ETHYL ESTER, M-METHYLCARBANILATE (ESTER);SN-38574;Ethyl N-[3-[N'-(3-methylphenyl)carbamoyloxy]phenyl]carbamate

Suppliers and Price of Phenmedipham-ethyl
Supply Marketing:
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
  • Sigma-Aldrich
  • Phenmedipham-ethyl PESTANAL
  • 25mg
  • $ 165.00
  • Crysdot
  • Ethyl(3-((m-tolylcarbamoyl)oxy)phenyl)carbamate 97%
  • 100mg
  • $ 316.00
  • American Custom Chemicals Corporation
  • PHENMEDIPHAM-ETHYL 95.00%
  • 5MG
  • $ 502.74
  • Ambeed
  • Ethyl(3-((m-tolylcarbamoyl)oxy)phenyl)carbamate 98%
  • 1g
  • $ 481.00
  • Ambeed
  • Ethyl(3-((m-tolylcarbamoyl)oxy)phenyl)carbamate 98%
  • 250mg
  • $ 204.00
  • Ambeed
  • Ethyl(3-((m-tolylcarbamoyl)oxy)phenyl)carbamate 98%
  • 100mg
  • $ 138.00
Total 21 raw suppliers
Chemical Property of Phenmedipham-ethyl
Chemical Property:
  • Vapor Pressure:8.75E-07mmHg at 25°C 
  • Melting Point:140-144 °C 
  • Refractive Index:1.628 
  • Boiling Point:405.5 °C at 760 mmHg 
  • PKA:12.96±0.70(Predicted) 
  • Flash Point:199 °C 
  • PSA:76.66000 
  • Density:1.274 g/cm3 
  • LogP:4.32030 
  • Storage Temp.:-20°C Freezer, Under inert atmosphere 
  • Solubility.:Chloroform (Slightly), Methanol (Slightly) 
  • XLogP3:4
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:6
  • Exact Mass:314.12665706
  • Heavy Atom Count:23
  • Complexity:402
Purity/Quality:

99% *data from raw suppliers

Phenmedipham-ethyl PESTANAL *data from reagent suppliers

Safty Information:
  • Pictogram(s):
  • Hazard Codes:
  • Statements: 50/53 
  • Safety Statements: 60-61 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC(=O)NC1=CC(=CC=C1)OC(=O)NC2=CC=CC(=C2)C
  • Uses Phenmedipham-ethyl is used as an agrochemical bioregulator. Phenmedipham-ethyl is an impurity of Phenmedipham (P314600); a carbanilate selective herbicide used post-emergence in beet crops after the emergence of most broad-leaved weeds and before they develop.
Technology Process of Phenmedipham-ethyl

There total 3 articles about Phenmedipham-ethyl 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:
Guidance literature:
Multi-step reaction with 2 steps
1: tetrahydrofuran / 2 h / 20 °C
2: triethylamine / benzene / 0.5 h / Reflux
With triethylamine; In tetrahydrofuran; benzene;
DOI:10.1016/j.bioorg.2018.03.012
Guidance literature:
Entspr. ROH (Acyl.);
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