C₁₉H₁₆FNO₅S

Base Information

Chemical Name:C₁₉H₁₆FNO₅S
CAS No.:1374233-07-4
Molecular Formula:C₁₉H₁₆FNO₅S
Molecular Weight:389.404
Hs Code.:

C<sub>19</sub>H<sub>16</sub>FNO<sub>5</sub>S

Synonyms:C₁₉H₁₆FNO₅S

Suppliers and Price of C₁₉H₁₆FNO₅S

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 C₁₉H₁₆FNO₅S

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₁₉H₁₆FNO₅S

There total 10 articles about C₁₉H₁₆FNO₅S 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: 100.0%

: 1374233-06-3
C₂₀H₁₈FNO₅S

: 1374233-07-4
C₁₉H₁₆FNO₅S

Guidance literature:: C₂₀H₁₈FNO₅S; With lithium hydroxide monohydrate; In tetrahydrofuran; methanol; at 70 ℃; for 1h;

With hydrogenchloride; In tetrahydrofuran; methanol; water; at 0 ℃;

Reference yield:

: 4964-76-5
7-methoxyquinoline

: 1374233-07-4
C₁₉H₁₆FNO₅S

Guidance literature:: Multi-step reaction with 9 steps

1.1: hydrogen / platinum(IV) oxide / methanol / 16 h / 20 °C

2.1: triethylamine / dichloromethane / 0.5 h / 0 - 20 °C

3.1: N-iodo-succinimide / chloroform / 16 h / 0 - 20 °C

4.1: boron tribromide / dichloromethane / 1 h / -20 °C

4.2: Cooling with ice

5.1: triethylamine / dmap / tetrahydrofuran / 3 h / 0 - 20 °C

6.1: piperidine / bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; tri-tert-butyl phosphine / N,N-dimethyl-formamide / 80 °C / Inert atmosphere

7.1: hydrogenchloride / 1,4-dioxane / 0.5 h / 20 °C

8.1: sodium acetate; potassium carbonate / copper dichloride; palladium dichloride / 20 °C

9.1: lithium hydroxide monohydrate / tetrahydrofuran; methanol / 1 h / 70 °C

9.2: 0 °C

With piperidine; hydrogenchloride; N-iodo-succinimide; lithium hydroxide monohydrate; hydrogen; sodium acetate; boron tribromide; potassium carbonate; triethylamine; dmap; platinum(IV) oxide; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; tri-tert-butyl phosphine; copper dichloride; palladium dichloride; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; chloroform; N,N-dimethyl-formamide;

Reference yield:

: 19500-61-9
7-methoxy-1,2,3,4-tetrahydroquinoline

: 1374233-07-4
C₁₉H₁₆FNO₅S

Guidance literature:: Multi-step reaction with 8 steps

1.1: triethylamine / dichloromethane / 0.5 h / 0 - 20 °C

2.1: N-iodo-succinimide / chloroform / 16 h / 0 - 20 °C

3.1: boron tribromide / dichloromethane / 1 h / -20 °C

3.2: Cooling with ice

4.1: triethylamine / dmap / tetrahydrofuran / 3 h / 0 - 20 °C

5.1: piperidine / bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; tri-tert-butyl phosphine / N,N-dimethyl-formamide / 80 °C / Inert atmosphere

6.1: hydrogenchloride / 1,4-dioxane / 0.5 h / 20 °C

7.1: sodium acetate; potassium carbonate / copper dichloride; palladium dichloride / 20 °C

8.1: lithium hydroxide monohydrate / tetrahydrofuran; methanol / 1 h / 70 °C

8.2: 0 °C

With piperidine; hydrogenchloride; N-iodo-succinimide; lithium hydroxide monohydrate; sodium acetate; boron tribromide; potassium carbonate; triethylamine; dmap; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; tri-tert-butyl phosphine; copper dichloride; palladium dichloride; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; chloroform; N,N-dimethyl-formamide;