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Benzoic acid, 2-aMino-4-Methoxy-5-[3-(4-Morpholinyl)propoxy]-, Methyl ester

Base Information Edit
  • Chemical Name:Benzoic acid, 2-aMino-4-Methoxy-5-[3-(4-Morpholinyl)propoxy]-, Methyl ester
  • CAS No.:214472-41-0
  • Molecular Formula:C16H24N2O5
  • Molecular Weight:324.377
  • Hs Code.:
  • Mol file:214472-41-0.mol
Benzoic acid, 2-aMino-4-Methoxy-5-[3-(4-Morpholinyl)propoxy]-, Methyl ester

Synonyms:methyl 2-amino-4-methoxy-5-(3-morpholin-4-yl-propoxy)benzoate; Benzoic acid, 2-amino-4-methoxy-5-[3-(4-morpholinyl)propoxy]-, methyl ester; methyl 2-amino-4-methoxy-5-(3-morpholinopropoxy)benzoate; 2-amino-4-methoxy-5-(3-morpholin-4-ylpropoxy)benzoic acid methyl ester; methyl 2-amino-4-methoxy-3-(3-morpholinopropoxy)benzoate;

Suppliers and Price of Benzoic acid, 2-aMino-4-Methoxy-5-[3-(4-Morpholinyl)propoxy]-, Methyl ester
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
Total 10 raw suppliers
Chemical Property of Benzoic acid, 2-aMino-4-Methoxy-5-[3-(4-Morpholinyl)propoxy]-, Methyl ester Edit
Chemical Property:
  • PSA:83.25000 
  • LogP:1.68420 
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of Benzoic acid, 2-aMino-4-Methoxy-5-[3-(4-Morpholinyl)propoxy]-, Methyl ester

There total 7 articles about Benzoic acid, 2-aMino-4-Methoxy-5-[3-(4-Morpholinyl)propoxy]-, Methyl ester 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 hydrogen; palladium 10% on activated carbon; In ethyl acetate; for 3h; under 3345.86 Torr;
Guidance literature:
Multi-step reaction with 4 steps
1: 76 percent / potassium carbonate / acetone / 24 h / Heating
2: 82 percent / nitric acid; trifluoroacetic acid / CH2Cl2 / 2 h / 20 °C
3: 60 percent / 1 h / 100 °C
4: hydrogen / palladium on activated carbon / methanol
With hydrogen; nitric acid; potassium carbonate; trifluoroacetic acid; palladium on activated charcoal; In methanol; dichloromethane; acetone;
DOI:10.1002/jlcr.998
Guidance literature:
Multi-step reaction with 4 steps
1: 99 percent / H2SO4 / Heating
2: 95 percent / tri-n-butyl ammonium iodide; K2CO3 / butan-2-one / Heating
3: 88 percent / HNO3; AcOH
4: 74 percent / H2 / Pd/C / ethanol; ethyl acetate
With sulfuric acid; hydrogen; nitric acid; tri-n-butylammonium iodide; potassium carbonate; acetic acid; palladium on activated charcoal; In ethanol; ethyl acetate; butanone; 1: Fisher esterification;
DOI:10.1016/S0960-894X(02)00598-X
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