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Methyl 2-CarbaMoylbenzoate

Base Information Edit
  • Chemical Name:Methyl 2-CarbaMoylbenzoate
  • CAS No.:90564-02-6
  • Molecular Formula:C9H9NO3
  • Molecular Weight:179.17266
  • Hs Code.:2924299090
  • Mol file:90564-02-6.mol
Methyl 2-CarbaMoylbenzoate

Synonyms:Methyl 2-CarbaMoylbenzoate;2-(Aminocarbonyl)benzoic acid methyl ester

Suppliers and Price of Methyl 2-CarbaMoylbenzoate
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
  • SynQuest Laboratories
  • Methyl 2-carbamoylbenzoate
  • 5 g
  • $ 1456.00
  • Crysdot
  • Methyl2-Carbamoylbenzoate 95+%
  • 5g
  • $ 611.00
  • Ambeed
  • Methyl2-Carbamoylbenzoate 95+%
  • 1g
  • $ 196.00
  • Ambeed
  • Methyl2-Carbamoylbenzoate 95+%
  • 250mg
  • $ 79.00
  • Ambeed
  • Methyl2-Carbamoylbenzoate 95+%
  • 100mg
  • $ 45.00
  • AK Scientific
  • Methyl2-carbamoylbenzoate
  • 5g
  • $ 937.00
Total 6 raw suppliers
Chemical Property of Methyl 2-CarbaMoylbenzoate Edit
Chemical Property:
  • PSA:70.38000 
  • LogP:1.45630 
  • Storage Temp.:Sealed in dry,Room Temperature 
Purity/Quality:

98%min *data from raw suppliers

Methyl 2-carbamoylbenzoate *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of Methyl 2-CarbaMoylbenzoate

There total 9 articles about Methyl 2-CarbaMoylbenzoate 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 titanium(III) chloride; In ethanol; at 25 ℃; for 16h;
DOI:10.1021/jo00066a014
Guidance literature:
With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 3h;
DOI:10.1021/acs.orglett.0c03897
Guidance literature:
With sulfuric acid; 1,1,1,3,3,3-hexamethyl-disilazane; Yield given. Multistep reaction; 1.) CH2Cl2, room temp., 2.) CH3OH;
DOI:10.1055/s-1985-31257
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