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2-Acetyl-4-Methylphenyl Benzoate

Base Information
  • Chemical Name:2-Acetyl-4-Methylphenyl Benzoate
  • CAS No.:4010-19-9
  • Molecular Formula:C16H14O3
  • Molecular Weight:254.285
  • Hs Code.:
  • Mol file:4010-19-9.mol
2-Acetyl-4-Methylphenyl Benzoate

Synonyms:

Suppliers and Price of 2-Acetyl-4-Methylphenyl Benzoate
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
  • Crysdot
  • 2-Acetyl-4-methylphenylbenzoate 95+%
  • 5g
  • $ 892.00
  • Crysdot
  • 2-Acetyl-4-methylphenylbenzoate 95+%
  • 1g
  • $ 297.00
Total 4 raw suppliers
Chemical Property of 2-Acetyl-4-Methylphenyl Benzoate
Chemical Property:
  • PSA:43.37000 
  • LogP:3.41680 
Purity/Quality:

95% *data from raw suppliers

2-Acetyl-4-methylphenylbenzoate 95+% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 2-Acetyl-4-Methylphenyl Benzoate

There total 6 articles about 2-Acetyl-4-Methylphenyl 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:
With pyridine; at 70 ℃; for 0.166667h;
DOI:10.1246/cl.2007.522
Guidance literature:
With tert.-butylhydroperoxide; copper(II) acetate dihydrate; In decane; at 120 ℃; for 3h; chemoselective reaction;
DOI:10.1021/ol401682a
Guidance literature:
Multi-step reaction with 3 steps
1: pyridine
2: AlCl3
3: pyridine
With pyridine; aluminium trichloride; 2: Fries rearrangement / 3: Schotten-Baumann reaction;
DOI:10.1021/jm020839k
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