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1-Benzyl-2,4-diphenyl-1H-pyrrole

Base Information
  • Chemical Name:1-Benzyl-2,4-diphenyl-1H-pyrrole
  • CAS No.:15811-38-8
  • Molecular Formula:C23H19N
  • Molecular Weight:309.411
  • Hs Code.:
  • Mol file:15811-38-8.mol
1-Benzyl-2,4-diphenyl-1H-pyrrole

Synonyms:1-Benzyl-2,4-diphenyl-1H-pyrrole

Suppliers and Price of 1-Benzyl-2,4-diphenyl-1H-pyrrole
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 1-Benzyl-2,4-diphenyl-1H-pyrrole
Chemical Property:
  • PSA:4.93000 
  • LogP:5.87040 
Purity/Quality:
Safty Information:
  • Pictogram(s):  
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MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 1-Benzyl-2,4-diphenyl-1H-pyrrole

There total 3 articles about 1-Benzyl-2,4-diphenyl-1H-pyrrole 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 2 steps
1: titanium(IV) tetraethanolate / n-heptane / Dean-Stark; Heating
2: palladium diacetate; tetrabutylammomium bromide; oxygen; Trimethylacetic acid / dimethyl sulfoxide / 24 h / 80 °C / Schlenk technique; Molecular sieve
With titanium(IV) tetraethanolate; tetrabutylammomium bromide; oxygen; palladium diacetate; Trimethylacetic acid; In n-heptane; dimethyl sulfoxide;
DOI:10.1016/j.tetlet.2020.151887
Guidance literature:
Multi-step reaction with 3 steps
2: potassium hydroxide / tetrahydrofuran; methanol; water / 36 h / 50 °C
3: trifluoroacetic anhydride / dichloromethane / 20 h / 20 °C
With trifluoroacetic anhydride; potassium hydroxide; In tetrahydrofuran; methanol; dichloromethane; water; 1: |Paal-Knorr Pyrrole Synthesis / 3: |Friedel-Crafts Acylation;
DOI:10.5012/bkcs.2013.34.9.2604
Guidance literature:
Multi-step reaction with 3 steps
2: potassium hydroxide / tetrahydrofuran; methanol; water / 36 h / 50 °C
3: trifluoroacetic anhydride / dichloromethane / 20 h / 20 °C
With trifluoroacetic anhydride; potassium hydroxide; In tetrahydrofuran; methanol; dichloromethane; water; 1: |Paal-Knorr Pyrrole Synthesis / 3: |Friedel-Crafts Acylation;
DOI:10.5012/bkcs.2013.34.9.2604
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