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2-(4-PIPERAZIN-1-YL-PHENYL)-BENZOOXAZOLE

Base Information Edit
  • Chemical Name:2-(4-PIPERAZIN-1-YL-PHENYL)-BENZOOXAZOLE
  • CAS No.:885275-02-5
  • Molecular Formula:C17H17 N3 O
  • Molecular Weight:279.34
  • Hs Code.:2934999090
  • Mol file:885275-02-5.mol
2-(4-PIPERAZIN-1-YL-PHENYL)-BENZOOXAZOLE

Synonyms:2-(4-PIPERAZIN-1-YL-PHENYL)-BENZOOXAZOLE

Suppliers and Price of 2-(4-PIPERAZIN-1-YL-PHENYL)-BENZOOXAZOLE
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
  • J&W Pharmlab
  • 2-(4-Piperazin-1-yl-phenyl)-benzooxazole 96%
  • 5g
  • $ 5880.00
  • Crysdot
  • 2-(4-(Piperazin-1-yl)phenyl)benzo[d]oxazole 95+%
  • 1g
  • $ 880.00
  • Chemenu
  • 2-(4-Piperazin-1-yl-phenyl)-benzooxazole 95%
  • 1g
  • $ 830.00
Total 6 raw suppliers
Chemical Property of 2-(4-PIPERAZIN-1-YL-PHENYL)-BENZOOXAZOLE Edit
Chemical Property:
  • PSA:41.30000 
  • LogP:3.29820 
Purity/Quality:

98% *data from raw suppliers

2-(4-Piperazin-1-yl-phenyl)-benzooxazole 96% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 2-(4-PIPERAZIN-1-YL-PHENYL)-BENZOOXAZOLE

There total 3 articles about 2-(4-PIPERAZIN-1-YL-PHENYL)-BENZOOXAZOLE 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 trifluoroacetic acid; In dichloromethane; at 0 - 20 ℃; for 3h; Inert atmosphere;
DOI:10.1021/ml300472n
Guidance literature:
Multi-step reaction with 2 steps
1: 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; oxygen / toluene / 12 h / 120 °C
2: trifluoroacetic acid / dichloromethane / 3 h / 0 - 20 °C / Inert atmosphere
With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; oxygen; trifluoroacetic acid; In dichloromethane; toluene;
DOI:10.1021/ml300472n
Guidance literature:
Multi-step reaction with 2 steps
1: 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; oxygen / toluene / 12 h / 120 °C
2: trifluoroacetic acid / dichloromethane / 3 h / 0 - 20 °C / Inert atmosphere
With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; oxygen; trifluoroacetic acid; In dichloromethane; toluene;
DOI:10.1021/ml300472n
Refernces Edit
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