Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

C22H16F2N2O2

Base Information Edit
  • Chemical Name:C22H16F2N2O2
  • CAS No.:1417404-29-5
  • Molecular Formula:C22H16F2N2O2
  • Molecular Weight:378.378
  • Hs Code.:
  • Mol file:1417404-29-5.mol
C<sub>22</sub>H<sub>16</sub>F<sub>2</sub>N<sub>2</sub>O<sub>2</sub>

Synonyms:

Suppliers and Price of C22H16F2N2O2
Supply Marketing:Edit
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 C22H16F2N2O2 Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of C22H16F2N2O2

There total 15 articles about C22H16F2N2O2 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:
Guidance literature:
Multi-step reaction with 7 steps
1: aluminum (III) chloride / dichloromethane / 0.33 h / 0 °C
2: thionyl chloride / dichloromethane / 1 h / Reflux
3: dichloromethane / 0 - 20 °C
4: palladium diacetate; XPhos; potassium tert-butylate / toluene; tert-butyl alcohol / 2 h / 100 °C / Inert atmosphere
5: hydrogenchloride; water / 6 h / Reflux
6: tetrahydrofuran / 1.5 h / 20 °C
7: ammonia / 20 °C
With hydrogenchloride; aluminum (III) chloride; thionyl chloride; potassium tert-butylate; ammonia; water; palladium diacetate; XPhos; In tetrahydrofuran; dichloromethane; toluene; tert-butyl alcohol; 1: |Friedel-Crafts Acylation / 4: |Buchwald-Hartwig Coupling;
DOI:10.1021/jm301539x
Guidance literature:
Multi-step reaction with 5 steps
1: dichloromethane / 0 - 20 °C
2: palladium diacetate; XPhos; potassium tert-butylate / toluene; tert-butyl alcohol / 2 h / 100 °C / Inert atmosphere
3: hydrogenchloride; water / 6 h / Reflux
4: tetrahydrofuran / 1.5 h / 20 °C
5: ammonia / 20 °C
With hydrogenchloride; potassium tert-butylate; ammonia; water; palladium diacetate; XPhos; In tetrahydrofuran; dichloromethane; toluene; tert-butyl alcohol; 2: |Buchwald-Hartwig Coupling;
DOI:10.1021/jm301539x
Guidance literature:
With ammonia; at 20 ℃;
DOI:10.1021/jm301539x
Post RFQ for Price