C₂₆H₂₇F₂NO₃

Base Information

Chemical Name:C₂₆H₂₇F₂NO₃
CAS No.:1427406-37-8
Molecular Formula:C₂₆H₂₇F₂NO₃
Molecular Weight:439.502
Hs Code.:

C<sub>26</sub>H<sub>27</sub>F<sub>2</sub>NO<sub>3</sub>

Synonyms:C₂₆H₂₇F₂NO₃

Suppliers and Price of C₂₆H₂₇F₂NO₃

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 C₂₆H₂₇F₂NO₃

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₆H₂₇F₂NO₃

There total 16 articles about C₂₆H₂₇F₂NO₃ 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: 90.0%

: 1427406-10-7
2-[3-[[2-fluoro-5-(3-fluorophenyl)phenyl]methylamino]-2,4-dimethylphenoxy]acetic acid

: 67-63-0,8013-70-5
isopropyl alcohol

: 1427406-37-8
C₂₆H₂₇F₂NO₃

Guidance literature:: With thionyl chloride; for 2h; Reflux;

Reference yield:

: 87-62-7
2,6-dimethylaniline

: 1427406-37-8
C₂₆H₂₇F₂NO₃

Guidance literature:: Multi-step reaction with 12 steps

1.1: 1 h / 0 - 20 °C

2.1: nitric acid; acetic acid; sulfuric acid / 1 h / 0 - 20 °C

3.1: palladium 10% on activated carbon; hydrogen / ethanol; methanol; acetic acid / 36 h / 20 °C

4.1: sodium nitrite; sulfuric acid / water / 0.5 h / 0 °C

4.2: 2 h / 100 °C

5.1: dmap; triethylamine / N,N-dimethyl-formamide / 50 °C

6.1: hydrazine hydrate / tert-butyl alcohol / 110 °C / Inert atmosphere

7.1: trifluoroacetic acid / dichloromethane / 20 °C

8.1: sodium hydrogencarbonate / tetrahydrofuran / 0.5 h / 20 °C

9.1: borane-THF / tetrahydrofuran / 3 h / 60 °C / Inert atmosphere

10.1: caesium carbonate / butanone / 0.5 h / 20 °C

10.2: 3 h / 20 °C

11.1: water; sodium hydroxide / tetrahydrofuran / 1 h / 20 °C

12.1: thionyl chloride / 2 h / Reflux

With dmap; thionyl chloride; borane-THF; sulfuric acid; palladium 10% on activated carbon; water; hydrogen; nitric acid; sodium hydrogencarbonate; caesium carbonate; hydrazine hydrate; acetic acid; triethylamine; trifluoroacetic acid; sodium hydroxide; sodium nitrite; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; acetic acid; N,N-dimethyl-formamide; butanone; tert-butyl alcohol;

Reference yield:

: 2198-53-0
N-(2,6-dimethylphenyl)acetamide

: 1427406-37-8
C₂₆H₂₇F₂NO₃

Guidance literature:: Multi-step reaction with 11 steps

1.1: nitric acid; acetic acid; sulfuric acid / 1 h / 0 - 20 °C

2.1: palladium 10% on activated carbon; hydrogen / ethanol; methanol; acetic acid / 36 h / 20 °C

3.1: sodium nitrite; sulfuric acid / water / 0.5 h / 0 °C

3.2: 2 h / 100 °C

4.1: dmap; triethylamine / N,N-dimethyl-formamide / 50 °C

5.1: hydrazine hydrate / tert-butyl alcohol / 110 °C / Inert atmosphere

6.1: trifluoroacetic acid / dichloromethane / 20 °C

7.1: sodium hydrogencarbonate / tetrahydrofuran / 0.5 h / 20 °C

8.1: borane-THF / tetrahydrofuran / 3 h / 60 °C / Inert atmosphere

9.1: caesium carbonate / butanone / 0.5 h / 20 °C

9.2: 3 h / 20 °C

10.1: water; sodium hydroxide / tetrahydrofuran / 1 h / 20 °C

11.1: thionyl chloride / 2 h / Reflux

With dmap; thionyl chloride; borane-THF; sulfuric acid; palladium 10% on activated carbon; water; hydrogen; nitric acid; sodium hydrogencarbonate; caesium carbonate; hydrazine hydrate; acetic acid; triethylamine; trifluoroacetic acid; sodium hydroxide; sodium nitrite; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; acetic acid; N,N-dimethyl-formamide; butanone; tert-butyl alcohol;