Cyclohexanone, 3-[[4-(1,1-dimethylethyl)phenyl]thio]-, (S)-

Base Information

Chemical Name:Cyclohexanone, 3-[[4-(1,1-dimethylethyl)phenyl]thio]-, (S)-
CAS No.:113036-75-2
Molecular Formula:C16H22OS
Molecular Weight:262.416
Hs Code.:

Synonyms:

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

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Chemical Property of Cyclohexanone, 3-[[4-(1,1-dimethylethyl)phenyl]thio]-, (S)-

Chemical Property:

Purity/Quality:

Safty Information:

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MSDS Files:: SDS file from LookChem

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Technology Process of Cyclohexanone, 3-[[4-(1,1-dimethylethyl)phenyl]thio]-, (S)-

There total 4 articles about Cyclohexanone, 3-[[4-(1,1-dimethylethyl)phenyl]thio]-, (S)- 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%

: 930-68-7
cyclohexenone

: 2396-68-1
4-t-butylbenzenethiol

: 113036-75-2
(S)-3-(4-tert-butylphenylthio)-cyclohexanone

Guidance literature:: With 1-(3,5-bis(trifluoromethyl)phenyl)-3-((S)-(6-methoxyquinolin-4-yl)((2S,4S,8R)-8-vinylquinuclidin-2-yl)methyl)urea; In toluene; at 20 ℃; for 8h; optical yield given as %ee; enantioselective reaction;
DOI:10.1021/jo902634a

Reference yield: 98.0%

: 930-68-7
cyclohexenone

: 2396-68-1
4-t-butylbenzenethiol

: 64888-90-0,113036-75-2,116403-76-0,36674-55-2
rac-3-(4-tert-butylphenylthio)-cyclohexanone

Guidance literature:: With potassium fluoride; Quinine; In toluene; for 20h; Ambient temperature;

Reference yield:

: 930-68-7
cyclohexenone

: 2396-68-1
4-t-butylbenzenethiol

: 64888-90-0
(R)-3-(4-tert-butylphenylthio)-cyclohexanone

: 113036-75-2
(S)-3-(4-tert-butylphenylthio)-cyclohexanone

Guidance literature:: With Cinchonidin; In benzene; at 22 ℃; for 15h; Product distribution; Mechanism; stereoselectivity, different enones, catalysts, solvents and temperatures;
DOI:10.1021/ja00392a029