1-Propanone, 2-[[(4-methylphenyl)sulfonyl]oxy]-1-phenyl-

Base Information

Chemical Name:1-Propanone, 2-[[(4-methylphenyl)sulfonyl]oxy]-1-phenyl-
CAS No.:87456-64-2
Molecular Formula:C16H16O4S
Molecular Weight:304.367
Hs Code.:
DSSTox Substance ID:DTXSID20431913
Nikkaji Number:J1.002.663F

Synonyms:1-Propanone, 2-[[(4-methylphenyl)sulfonyl]oxy]-1-phenyl-;alpha-(Tosyloxy)propiophenone;87456-64-2;SCHEMBL3096091;DTXSID20431913

Suppliers and Price of 1-Propanone, 2-[[(4-methylphenyl)sulfonyl]oxy]-1-phenyl-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemicals and raw materials
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Total 0 raw suppliers

Chemical Property of 1-Propanone, 2-[[(4-methylphenyl)sulfonyl]oxy]-1-phenyl-

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:304.07693016
Heavy Atom Count:21
Complexity:437

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)OC(C)C(=O)C2=CC=CC=C2

Technology Process of 1-Propanone, 2-[[(4-methylphenyl)sulfonyl]oxy]-1-phenyl-

There total 26 articles about 1-Propanone, 2-[[(4-methylphenyl)sulfonyl]oxy]-1-phenyl- 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:

Reference yield: 99.0%

: 104-15-4
toluene-4-sulfonic acid

: 93-55-0
1-phenyl-propan-1-one

: 87456-64-2
α-tosyloxypropiophenone

Guidance literature:: With N-butyl-5-iodo-2-methoxybenzamide; 3-chloro-benzenecarboperoxoic acid; In acetonitrile; at 50 ℃; for 24h; Temperature; Reagent/catalyst; enantioselective reaction;
DOI:10.1021/acs.joc.5b02129