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N-Ethylacetanilide

Base Information Edit
  • Chemical Name:N-Ethylacetanilide
  • CAS No.:529-65-7
  • Molecular Formula:C10H13 N O
  • Molecular Weight:163.219
  • Hs Code.:2924299090
  • European Community (EC) Number:208-466-9
  • NSC Number:8737
  • DSSTox Substance ID:DTXSID1060186
  • Nikkaji Number:J6.689C
  • Wikidata:Q22829157
  • Mol file:529-65-7.mol
N-Ethylacetanilide

Synonyms:N-ethylacetanilide

Suppliers and Price of N-Ethylacetanilide
Supply Marketing:Edit
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
  • American Custom Chemicals Corporation
  • N-ETHYL-N-PHENYLACETAMIDE 95.00%
  • 5MG
  • $ 501.56
  • AHH
  • N-Ethylacetanilide 98%
  • 1000g
  • $ 435.00
Total 10 raw suppliers
Chemical Property of N-Ethylacetanilide Edit
Chemical Property:
  • Vapor Pressure:0.0288mmHg at 25°C 
  • Melting Point:55°C 
  • Refractive Index:1.5718 (estimate) 
  • Boiling Point:245.4°C at 760 mmHg 
  • PKA:0.54±0.50(Predicted) 
  • Flash Point:101.4°C 
  • PSA:20.31000 
  • Density:1.035g/cm3 
  • LogP:2.05940 
  • XLogP3:1.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:2
  • Exact Mass:163.099714038
  • Heavy Atom Count:12
  • Complexity:150
Purity/Quality:

99.5% *data from raw suppliers

N-ETHYL-N-PHENYLACETAMIDE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CCN(C1=CC=CC=C1)C(=O)C
  • Uses Substitute for camphor in nitrocellulose.
Technology Process of N-Ethylacetanilide

There total 37 articles about N-Ethylacetanilide 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:
With potassium phosphate; 4,5-dimethyl-1,3-bis-(2,4,6-trimethylphenyl)-3H-imidazol-1-ium chloride; C46H39ClNiP2; isopropyl alcohol; In toluene; at 100 ℃; for 15.15h;
DOI:10.1055/a-1548-8362
Guidance literature:
With mercury(II) diacetate; In tetrahydrofuran; for 4h; Ambient temperature;
Guidance literature:
With oxygen; copper diacetate; at 85 ℃; for 36h; Schlenk technique; Sealed tube;
DOI:10.1039/c5cc07454a
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