C₂₂H₂₆FNO₅S

Base Information

Chemical Name:C₂₂H₂₆FNO₅S
CAS No.:1193512-78-5
Molecular Formula:C₂₂H₂₆FNO₅S
Molecular Weight:435.517
Hs Code.:

C<sub>22</sub>H<sub>26</sub>FNO<sub>5</sub>S

Synonyms:C₂₂H₂₆FNO₅S

Suppliers and Price of C₂₂H₂₆FNO₅S

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 0 raw suppliers

Chemical Property of C₂₂H₂₆FNO₅S

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₂H₂₆FNO₅S

There total 13 articles about C₂₂H₂₆FNO₅S 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: 45.0%

: 1193512-77-4
C₂₂H₂₆FNO₅S

: 1193512-78-5
C₂₂H₂₆FNO₅S

: 1193512-79-6
C₂₂H₂₆FNO₅S

Guidance literature:: C₂₂H₂₆FNO₅S; With potassium tert-butylate; In tetrahydrofuran; at 0 ℃; for 1h;

With acetic acid; In tetrahydrofuran;

Reference yield:

: 540-36-3
para-difluorobenzene

: 1193512-78-5
C₂₂H₂₆FNO₅S

: 1193512-79-6
C₂₂H₂₆FNO₅S

Guidance literature:: Multi-step reaction with 6 steps

1.1: aluminum (III) chloride / 16 h / 20 °C / Reflux

2.1: potassium carbonate; tetrabutylammomium bromide / toluene / 24 h / Reflux

2.2: 12 h

2.3: 1.5 h

3.1: boron trifluoride diethyl etherate; triethylsilane / 8 h / 65 °C

4.1: potassium carbonate / acetonitrile; ethanol; water / 5 °C

4.2: 1 h

5.1: sodium hydrogencarbonate; 4-acetylamino-2,2,6,6-tetramethyl-1-piperidinoxy; sodium hypochlorite; sodium bromide / dichloromethane; water / 2 h

6.1: potassium tert-butylate / tetrahydrofuran / 1 h / 0 °C

With triethylsilane; aluminum (III) chloride; sodium hypochlorite; boron trifluoride diethyl etherate; 4-acetylamino-2,2,6,6-tetramethyl-1-piperidinoxy; potassium tert-butylate; tetrabutylammomium bromide; sodium hydrogencarbonate; potassium carbonate; sodium bromide; In tetrahydrofuran; ethanol; dichloromethane; water; toluene; acetonitrile;

Reference yield:

: 121-90-4
m-nitrobenzoic acid chloride

: 1193512-78-5
C₂₂H₂₆FNO₅S

: 1193512-79-6
C₂₂H₂₆FNO₅S

Guidance literature:: Multi-step reaction with 6 steps

1.1: aluminum (III) chloride / 16 h / 20 °C / Reflux

2.1: potassium carbonate; tetrabutylammomium bromide / toluene / 24 h / Reflux

2.2: 12 h

2.3: 1.5 h

3.1: boron trifluoride diethyl etherate; triethylsilane / 8 h / 65 °C

4.1: potassium carbonate / acetonitrile; ethanol; water / 5 °C

4.2: 1 h

5.1: sodium hydrogencarbonate; 4-acetylamino-2,2,6,6-tetramethyl-1-piperidinoxy; sodium hypochlorite; sodium bromide / dichloromethane; water / 2 h

6.1: potassium tert-butylate / tetrahydrofuran / 1 h / 0 °C

With triethylsilane; aluminum (III) chloride; sodium hypochlorite; boron trifluoride diethyl etherate; 4-acetylamino-2,2,6,6-tetramethyl-1-piperidinoxy; potassium tert-butylate; tetrabutylammomium bromide; sodium hydrogencarbonate; potassium carbonate; sodium bromide; In tetrahydrofuran; ethanol; dichloromethane; water; toluene; acetonitrile;