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ethyl 3,5-dimethylbenzene-1-carboximidate

Base Information
  • Chemical Name:ethyl 3,5-dimethylbenzene-1-carboximidate
  • CAS No.:57312-28-4
  • Molecular Formula:C11H15NO
  • Molecular Weight:177.24300
  • Hs Code.:
  • Mol file:57312-28-4.mol
ethyl 3,5-dimethylbenzene-1-carboximidate

Synonyms:

Suppliers and Price of ethyl 3,5-dimethylbenzene-1-carboximidate
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
  • Labseeker
  • ethyl3,5-dimethylbenzene-1-carboximidate 95
  • 1g
  • $ 800.00
Total 4 raw suppliers
Chemical Property of ethyl 3,5-dimethylbenzene-1-carboximidate
Chemical Property:
  • Boiling Point:249.7±50.0 °C(Predicted) 
  • PKA:6.59±0.50(Predicted) 
  • PSA:33.08000 
  • Density:0.97±0.1 g/cm3(Predicted) 
  • LogP:2.76500 
Purity/Quality:

99% *data from raw suppliers

ethyl3,5-dimethylbenzene-1-carboximidate 95 *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of ethyl 3,5-dimethylbenzene-1-carboximidate

There total 2 articles about ethyl 3,5-dimethylbenzene-1-carboximidate 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:
In dichloromethane; at 20 ℃; for 34h; Inert atmosphere;
Guidance literature:
Multi-step reaction with 2 steps
1: ammonium hydroxide / dichloromethane / 1 h / 0 - 20 °C
2: dichloromethane / 4 h / 0 - 20 °C / Inert atmosphere
With ammonium hydroxide; In dichloromethane;
Guidance literature:
With zinc(II) chloride; In acetonitrile; at 80 ℃; for 12h; Schlenk technique;
DOI:10.1021/acs.joc.8b02437
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