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3-(benzoylamino)-4-methylbenzoic acid

Base Information Edit
  • Chemical Name:3-(benzoylamino)-4-methylbenzoic acid
  • CAS No.:401828-76-0
  • Molecular Formula:C15H13NO3
  • Molecular Weight:255.273
  • Hs Code.:
  • Mol file:401828-76-0.mol
3-(benzoylamino)-4-methylbenzoic acid

Synonyms:

Suppliers and Price of 3-(benzoylamino)-4-methylbenzoic acid
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
  • Matrix Scientific
  • 3-(Benzoylamino)-4-methylbenzoic acid
  • 500mg
  • $ 158.00
  • Crysdot
  • 3-Benzamido-4-methylbenzoicacid 97%
  • 5g
  • $ 527.00
  • Biosynth Carbosynth
  • 3-(Benzoylamino)-4-methylbenzoic acid
  • 5 g
  • $ 578.00
  • Biosynth Carbosynth
  • 3-(Benzoylamino)-4-methylbenzoic acid
  • 1 g
  • $ 170.00
  • Biosynth Carbosynth
  • 3-(Benzoylamino)-4-methylbenzoic acid
  • 500 mg
  • $ 100.00
  • Biosynth Carbosynth
  • 3-(Benzoylamino)-4-methylbenzoic acid
  • 250 mg
  • $ 57.50
  • Biosynth Carbosynth
  • 3-(Benzoylamino)-4-methylbenzoic acid
  • 2 g
  • $ 289.00
  • AK Scientific
  • 3-(Benzoylamino)-4-methylbenzoicacid
  • 500mg
  • $ 185.00
Total 2 raw suppliers
Chemical Property of 3-(benzoylamino)-4-methylbenzoic acid Edit
Chemical Property:
  • Boiling Point:367.2±35.0 °C(Predicted) 
  • PKA:4.35±0.10(Predicted) 
  • Density:1.295±0.06 g/cm3(Predicted) 
Purity/Quality:

98%min *data from raw suppliers

3-(Benzoylamino)-4-methylbenzoic acid *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 3-(benzoylamino)-4-methylbenzoic acid

There total 2 articles about 3-(benzoylamino)-4-methylbenzoic acid 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:
Multi-step reaction with 3 steps
1: thionyl chloride / 1 h / 0 °C / Reflux
2: benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 20 °C
3: sodium hydroxide; water / methanol / 2 h / 50 °C
With thionyl chloride; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; water; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; methanol;
DOI:10.1021/acs.jmedchem.5b01478
Guidance literature:
Multi-step reaction with 2 steps
1: benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 20 °C
2: sodium hydroxide; water / methanol / 2 h / 50 °C
With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; water; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; methanol;
DOI:10.1021/acs.jmedchem.5b01478
Guidance literature:
Multi-step reaction with 2 steps
1: triethylamine / tetrahydrofuran / 0.5 h / 0 - 20 °C
2: hydroxylamine / tetrahydrofuran; methanol
With hydroxylamine; triethylamine; In tetrahydrofuran; methanol;
DOI:10.1021/acs.jmedchem.5b01478
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