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2-(1,3,4-OXADIAZOL-2-YL)PHENYL BENZENECARBOXYLATE

Base Information
  • Chemical Name:2-(1,3,4-OXADIAZOL-2-YL)PHENYL BENZENECARBOXYLATE
  • CAS No.:240115-75-7
  • Molecular Formula:C15H10N2O3
  • Molecular Weight:266.256
  • Hs Code.:
  • Mol file:240115-75-7.mol
2-(1,3,4-OXADIAZOL-2-YL)PHENYL BENZENECARBOXYLATE

Synonyms:

Suppliers and Price of 2-(1,3,4-OXADIAZOL-2-YL)PHENYL BENZENECARBOXYLATE
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
  • American Custom Chemicals Corporation
  • 2-(1,3,4-OXADIAZOL-2-YL)PHENYL BENZENECARBOXYLATE 95.00%
  • 5MG
  • $ 687.35
  • American Custom Chemicals Corporation
  • 2-(1,3,4-OXADIAZOL-2-YL)PHENYL BENZENECARBOXYLATE 95.00%
  • 10MG
  • $ 679.14
  • American Custom Chemicals Corporation
  • 2-(1,3,4-OXADIAZOL-2-YL)PHENYL BENZENECARBOXYLATE 95.00%
  • 1MG
  • $ 647.61
Total 0 raw suppliers
Chemical Property of 2-(1,3,4-OXADIAZOL-2-YL)PHENYL BENZENECARBOXYLATE
Chemical Property:
Purity/Quality:

2-(1,3,4-OXADIAZOL-2-YL)PHENYL BENZENECARBOXYLATE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 2-(1,3,4-OXADIAZOL-2-YL)PHENYL BENZENECARBOXYLATE

There total 7 articles about 2-(1,3,4-OXADIAZOL-2-YL)PHENYL BENZENECARBOXYLATE 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:
With caesium carbonate; In N,N-dimethyl-formamide; at 70 ℃;
Guidance literature:
Multi-step reaction with 5 steps
1: hydrogen; palladium 10% on activated carbon / methanol; ethyl acetate / 1 h / 20 °C
2: 3 h / Reflux; Inert atmosphere
3: 1,8-diazabicyclo[5.4.0]undec-7-ene / iso-butanol / Inert atmosphere; Reflux
4: boron tribromide / chloroform / 2 h / -78 - 20 °C / Inert atmosphere
5: caesium carbonate / N,N-dimethyl-formamide / 70 °C
With palladium 10% on activated carbon; hydrogen; boron tribromide; caesium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In methanol; chloroform; ethyl acetate; N,N-dimethyl-formamide; iso-butanol;
Guidance literature:
Multi-step reaction with 4 steps
1: 3 h / Reflux; Inert atmosphere
2: 1,8-diazabicyclo[5.4.0]undec-7-ene / iso-butanol / Inert atmosphere; Reflux
3: boron tribromide / chloroform / 2 h / -78 - 20 °C / Inert atmosphere
4: caesium carbonate / N,N-dimethyl-formamide / 70 °C
With boron tribromide; caesium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In chloroform; N,N-dimethyl-formamide; iso-butanol;
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