C₅₉H₅₂Cl₂F₂N₂O₂₃

Base Information

Chemical Name:C₅₉H₅₂Cl₂F₂N₂O₂₃
CAS No.:1292322-48-5
Molecular Formula:C₅₉H₅₂Cl₂F₂N₂O₂₃
Molecular Weight:1265.96
Hs Code.:

C<sub>59</sub>H<sub>52</sub>Cl<sub>2</sub>F<sub>2</sub>N<sub>2</sub>O<sub>23</sub>

Synonyms:C₅₉H₅₂Cl₂F₂N₂O₂₃

Suppliers and Price of C₅₉H₅₂Cl₂F₂N₂O₂₃

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 C₅₉H₅₂Cl₂F₂N₂O₂₃

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₅₉H₅₂Cl₂F₂N₂O₂₃

There total 12 articles about C₅₉H₅₂Cl₂F₂N₂O₂₃ 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:

: 590-97-6
acetoxymethyl bromide

: C₄₄H₂₇Cl₂F₂N₂O₁₃^(5-)*5K⁽¹⁺⁾

: 1292322-48-5
C₅₉H₅₂Cl₂F₂N₂O₂₃

Guidance literature:: C₄₄H₂₇Cl₂F₂N₂O₁₃^(5-)*5K⁽¹⁺⁾; With hydrogenchloride; In water; pH=1.5;

acetoxymethyl bromide; With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃; for 2h;

Reference yield:

: 90162-13-3
methyl 6-hydroxy-1-naphthoate

: 1292322-48-5
C₅₉H₅₂Cl₂F₂N₂O₂₃

Guidance literature:: Multi-step reaction with 11 steps

1.1: Selectfluor / acetonitrile / 3 h / 20 °C

2.1: zinc; acetic acid

3.1: SEC-BUTYLAMINE; sulfuryl dichloride / toluene / 3 h / 66 °C

4.1: potassium carbonate / acetonitrile / 2 h / Reflux

5.1: lithium aluminium tetrahydride / diethyl ether / 0.5 h

6.1: pyridinium chlorochromate / dichloromethane / 2 h / 20 °C

7.1: 3-chloro-benzenecarboperoxoic acid; potassium hydroxide / benzene / 24 h / 70 °C

8.1: boron tribromide / dichloromethane / 3 h

8.2: Cooling with ice

9.1: methanesulfonic acid / 1 h / 20 °C

10.1: potassium hydroxide; water / methanol / 0.5 h / 20 °C

11.1: hydrogenchloride / water / pH 1.5

11.2: 2 h / 20 °C

With hydrogenchloride; lithium aluminium tetrahydride; sulfuryl dichloride; SEC-BUTYLAMINE; methanesulfonic acid; water; boron tribromide; potassium carbonate; acetic acid; Selectfluor; 3-chloro-benzenecarboperoxoic acid; pyridinium chlorochromate; potassium hydroxide; zinc; In methanol; diethyl ether; dichloromethane; water; toluene; acetonitrile; benzene; 7.1: Baeyer-Villager;

Reference yield:

: 388622-47-7
methyl 5-fluoro-6-hydroxy-1-naphthalenecarboxylate

: 1292322-48-5
C₅₉H₅₂Cl₂F₂N₂O₂₃

Guidance literature:: Multi-step reaction with 9 steps

1.1: SEC-BUTYLAMINE; sulfuryl dichloride / toluene / 3 h / 66 °C

2.1: potassium carbonate / acetonitrile / 2 h / Reflux

3.1: lithium aluminium tetrahydride / diethyl ether / 0.5 h

4.1: pyridinium chlorochromate / dichloromethane / 2 h / 20 °C

5.1: 3-chloro-benzenecarboperoxoic acid; potassium hydroxide / benzene / 24 h / 70 °C

6.1: boron tribromide / dichloromethane / 3 h

6.2: Cooling with ice

7.1: methanesulfonic acid / 1 h / 20 °C

8.1: potassium hydroxide; water / methanol / 0.5 h / 20 °C

9.1: hydrogenchloride / water / pH 1.5

9.2: 2 h / 20 °C

With hydrogenchloride; lithium aluminium tetrahydride; sulfuryl dichloride; SEC-BUTYLAMINE; methanesulfonic acid; water; boron tribromide; potassium carbonate; 3-chloro-benzenecarboperoxoic acid; pyridinium chlorochromate; potassium hydroxide; In methanol; diethyl ether; dichloromethane; water; toluene; acetonitrile; benzene; 5.1: Baeyer-Villager;