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5-phenyl-1-trityl-1H-tetrazole

Base Information Edit
  • Chemical Name:5-phenyl-1-trityl-1H-tetrazole
  • CAS No.:154750-11-5
  • Molecular Formula:C26H20N4
  • Molecular Weight:388.472
  • Hs Code.:
  • Mol file:154750-11-5.mol
5-phenyl-1-trityl-1H-tetrazole

Synonyms:5-phenyl-1-trityl-1H-tetrazole;2-Formyl-4-hydroxy-5-methoxyphenylboronic acid, pinacol ester

Suppliers and Price of 5-phenyl-1-trityl-1H-tetrazole
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
  • American Custom Chemicals Corporation
  • 5-PHENYL-1-TRITYL-1H-TETRAZOLE 95.00%
  • 5MG
  • $ 503.28
  • AK Scientific
  • 5-Phenyl-1-trityltetrazole
  • 5g
  • $ 937.00
Total 3 raw suppliers
Chemical Property of 5-phenyl-1-trityl-1H-tetrazole Edit
Chemical Property:
  • Boiling Point:586.1±60.0 °C(Predicted) 
  • PKA:0.37±0.10(Predicted) 
  • PSA:43.60000 
  • Density:1.14±0.1 g/cm3(Predicted) 
  • LogP:5.18030 
Purity/Quality:

99% *data from raw suppliers

5-PHENYL-1-TRITYL-1H-TETRAZOLE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 5-phenyl-1-trityl-1H-tetrazole

There total 3 articles about 5-phenyl-1-trityl-1H-tetrazole 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 tetrabutylammomium bromide; sodium carbonate; In chloroform; water; at 0 - 5 ℃; for 3 - 4h; Product distribution / selectivity;
Guidance literature:
Multi-step reaction with 2 steps
1: sodium azide; ammonium chloride / lithium chloride / N,N-dimethyl-formamide / 100 °C / Inert atmosphere
2: triethylamine / dichloromethane / 0 - 20 °C / Inert atmosphere
With sodium azide; ammonium chloride; triethylamine; lithium chloride; In dichloromethane; N,N-dimethyl-formamide;
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