O-isopropyl(Z)-S-4-phenylbut-3-enyl Dithiocarbonate

Base Information

Chemical Name:O-isopropyl(Z)-S-4-phenylbut-3-enyl Dithiocarbonate
CAS No.:119018-55-2
Molecular Formula:C₁₄H₁₈OS₂
Molecular Weight:266.428
Hs Code.:

Synonyms:O-isopropyl(Z)-S-4-phenylbut-3-enyl Dithiocarbonate

Suppliers and Price of O-isopropyl(Z)-S-4-phenylbut-3-enyl Dithiocarbonate

Supply Marketing:

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

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Total 1 raw suppliers

Chemical Property of O-isopropyl(Z)-S-4-phenylbut-3-enyl Dithiocarbonate

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of O-isopropyl(Z)-S-4-phenylbut-3-enyl Dithiocarbonate

There total 3 articles about O-isopropyl(Z)-S-4-phenylbut-3-enyl Dithiocarbonate 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: 89.0%

: 140-92-1
potassium isopropylxanthate

: 119018-54-1
(Z)-4-phenylbut-3-enyl methanesulphonate

: 119018-55-2
O-isopropyl(Z)-S-4-phenylbut-3-enyl Dithiocarbonate

Guidance literature:: tetrabutyl-ammonium chloride; In water; at 70 ℃; for 5h;

Reference yield:

: 10229-11-5
4-phenyl-but-3-yn-1-ol

: 119018-55-2
O-isopropyl(Z)-S-4-phenylbut-3-enyl Dithiocarbonate

Guidance literature:: Multi-step reaction with 3 steps

1: 88 percent / quinoline, hydrogen / palladium 5percent on barium sulphate / ethyl acetate / 5.5 h / 760 Torr

2: 94 percent / triethylamine / CH₂Cl₂

3: 89 percent / tetrabutylammonium chloride / H₂O / 5 h / 70 °C

With quinoline; hydrogen; triethylamine; palladium on barium sulfate; tetrabutyl-ammonium chloride; In dichloromethane; water; ethyl acetate;

Reference yield:

: 20047-19-2
(Z)-4-phenylbut-3-en-1-ol

: 119018-55-2
O-isopropyl(Z)-S-4-phenylbut-3-enyl Dithiocarbonate

Guidance literature:: Multi-step reaction with 2 steps

1: 94 percent / triethylamine / CH₂Cl₂

2: 89 percent / tetrabutylammonium chloride / H₂O / 5 h / 70 °C

With triethylamine; tetrabutyl-ammonium chloride; In dichloromethane; water;