(E)-2-(methylsulfonyl)-3-phenyl-2-propenyl alcohol

Base Information

Chemical Name:(E)-2-(methylsulfonyl)-3-phenyl-2-propenyl alcohol
CAS No.:197244-90-9
Molecular Formula:C₁₀H₁₂O₃S
Molecular Weight:212.269
Hs Code.:

Synonyms:(E)-2-(methylsulfonyl)-3-phenyl-2-propenyl alcohol

Suppliers and Price of (E)-2-(methylsulfonyl)-3-phenyl-2-propenyl alcohol

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

Total 1 raw suppliers

Chemical Property of (E)-2-(methylsulfonyl)-3-phenyl-2-propenyl alcohol

Chemical Property:

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (E)-2-(methylsulfonyl)-3-phenyl-2-propenyl alcohol

There total 1 articles about (E)-2-(methylsulfonyl)-3-phenyl-2-propenyl alcohol 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: 80.2%

: (E)-3-bromo-2-(methylsulfonyl)-1-phenyl-1-propene

: 197244-90-9
(E)-2-(methylsulfonyl)-3-phenyl-2-propenyl alcohol

Guidance literature:: With water; sodium formate; In methanol; for 6h; Heating;
DOI:10.1021/jo990541a

Reference yield: 86.4%

: 75-44-5
phosgene

: 197244-90-9
(E)-2-(methylsulfonyl)-3-phenyl-2-propenyl alcohol

: 252668-49-8
(E)-2-(methylsulfonyl)-3-phenyl-2-propenyl chloroformate

Guidance literature:: In tetrahydrofuran; at 20 ℃;
DOI:10.1021/jo990541a

Reference yield:

: 197244-90-9
(E)-2-(methylsulfonyl)-3-phenyl-2-propenyl alcohol

: Fluorocarbonylmethyl-carbamic acid (E)-2-methanesulfonyl-3-phenyl-allyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 86.4 percent / tetrahydrofuran / 20 °C

2: 75 percent / CH₂Cl₂

3: 84.4 percent / NaHCO₃ / H₂O; acetone

4: 82.5 percent / cyanuric fluoride; pyridine / CH₂Cl₂ / 1 h / 20 °C

With pyridine; trifluoro-[1,3,5]triazine; sodium hydrogencarbonate; In tetrahydrofuran; dichloromethane; water; acetone; 1: Substitution / 2: Substitution / 3: Substitution / 4: Fluorination;
DOI:10.1021/jo990541a