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methyl 2-[(4-methoxybenzoyl)amino]benzoate

Base Information Edit
  • Chemical Name:methyl 2-[(4-methoxybenzoyl)amino]benzoate
  • CAS No.:37619-28-6
  • Molecular Formula:C16H15NO4
  • Molecular Weight:285.299
  • Hs Code.:
  • Mol file:37619-28-6.mol
methyl 2-[(4-methoxybenzoyl)amino]benzoate

Synonyms:p-anisoyl amide of methyl anthranilate;methyl 2-(4-methoxybenzamido)benzoate;methyl N-(4-methoxybenzoyl)anthranilate;N-(4-methoxy-benzoyl)-anthranilic acid methyl ester;methyl N-p-anisoyl anthranilate;N-(4-Methoxy-benzoyl)-anthranilsaeure-methylester;

Suppliers and Price of methyl 2-[(4-methoxybenzoyl)amino]benzoate
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
  • METHYL 2-((4-METHOXYBENZOYL)AMINO)BENZOATE 95.00%
  • 5MG
  • $ 503.21
Total 0 raw suppliers
Chemical Property of methyl 2-[(4-methoxybenzoyl)amino]benzoate Edit
Chemical Property:
  • PSA:64.63000 
  • LogP:2.80710 
Purity/Quality:

METHYL 2-((4-METHOXYBENZOYL)AMINO)BENZOATE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of methyl 2-[(4-methoxybenzoyl)amino]benzoate

There total 3 articles about methyl 2-[(4-methoxybenzoyl)amino]benzoate 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:
Guidance literature:
With triethylamine; In dichloromethane; at 20 ℃; for 16h;
DOI:10.1021/jm990327e
Guidance literature:
Multi-step reaction with 2 steps
1: thionyl chloride / dichloromethane / 2 h / 20 °C
2: dichloromethane / 20 h / 20 °C
With thionyl chloride; In dichloromethane;
DOI:10.1007/s00044-012-0269-6
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