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Ethanone, 1-(4-methylphenyl)-, oxime, (1E)- (9CI)

Base Information Edit
  • Chemical Name:Ethanone, 1-(4-methylphenyl)-, oxime, (1E)- (9CI)
  • CAS No.:54582-23-9
  • Molecular Formula:C9H11NO
  • Molecular Weight:149.192
  • Hs Code.:
  • Mol file:54582-23-9.mol
Ethanone, 1-(4-methylphenyl)-, oxime, (1E)- (9CI)

Synonyms:Ethanone, 1-(4-methylphenyl)-, oxime, (1E)- (9CI)

Suppliers and Price of Ethanone, 1-(4-methylphenyl)-, oxime, (1E)- (9CI)
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
  • Crysdot
  • (E)-1-(p-Tolyl)ethanoneoxime 97%
  • 10g
  • $ 1439.00
  • Crysdot
  • (E)-1-(p-Tolyl)ethanoneoxime 97%
  • 5g
  • $ 972.00
  • Crysdot
  • (E)-1-(p-Tolyl)ethanoneoxime 97%
  • 1g
  • $ 446.00
Total 0 raw suppliers
Chemical Property of Ethanone, 1-(4-methylphenyl)-, oxime, (1E)- (9CI) Edit
Chemical Property:
  • PSA:32.59000 
  • LogP:2.19320 
Purity/Quality:

(E)-1-(p-Tolyl)ethanoneoxime 97% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of Ethanone, 1-(4-methylphenyl)-, oxime, (1E)- (9CI)

There total 5 articles about Ethanone, 1-(4-methylphenyl)-, oxime, (1E)- (9CI) 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 hydroxylamine hydrochloride; sodium acetate; In methanol; Heating;
DOI:10.1021/jo070297k

Reference yield: 99.0%

Guidance literature:
With ethyl acetohydroximate; scandium tris(trifluoromethanesulfonate); In ethanol; at 40 ℃; for 24h; stereoselective reaction; Inert atmosphere;
Guidance literature:
With Candida antarctica Lipase type B; urea hydrogen peroxide adduct; ethyl acetate; at 30 ℃; for 1h; under 760.051 Torr; Enzymatic reaction;
DOI:10.1039/c7ob00374a
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