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B3PYMPM

Base Information Edit
  • Chemical Name:B3PYMPM
  • CAS No.:925425-96-3
  • Molecular Formula:C37 H26 N6
  • Molecular Weight:554.654
  • Hs Code.:2933399990
  • Mol file:925425-96-3.mol
B3PYMPM

Synonyms:B3PYMPM;

Suppliers and Price of B3PYMPM
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
  • Chemenu
  • 4,6-Bis(3,5-di(pyridin-3-yl)phenyl)-2-methylpyrimidine 95%+
  • 250mg
  • $ 62.00
  • Chemenu
  • 4,6-Bis(3,5-di(pyridin-3-yl)phenyl)-2-methylpyrimidine 95%+
  • 1g
  • $ 281.00
  • Arctom
  • 4,6-Bis(3,5-di(pyridin-3-yl)phenyl)-2-methylpyrimidine 95%
  • 1g
  • $ 194.00
  • Arctom
  • 4,6-Bis(3,5-di(pyridin-3-yl)phenyl)-2-methylpyrimidine 95%
  • 250mg
  • $ 79.00
  • Arctom
  • 4,6-Bis(3,5-di(pyridin-3-yl)phenyl)-2-methylpyrimidine 95%
  • 100mg
  • $ 52.00
Total 26 raw suppliers
Chemical Property of B3PYMPM Edit
Chemical Property:
  • Boiling Point:772.1±55.0 °C(Predicted) 
  • PKA:4.79±0.12(Predicted) 
  • PSA:77.34000 
  • Density:1.214±0.06 g/cm3(Predicted) 
  • LogP:8.36700 
  • Storage Temp.:under inert gas (nitrogen or Argon) at 2-8°C 
Purity/Quality:

99% *data from raw suppliers

4,6-Bis(3,5-di(pyridin-3-yl)phenyl)-2-methylpyrimidine 95%+ *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Description B3PymPm is an isomer to?B2PymPm and?B4PymPm, with a 2-methylpyrimidine core structure with four pyridine pendants. It is electron-deficient and can be used in OLED devices as an electron-transporting or hole-blocking layer material.
Technology Process of B3PYMPM

There total 3 articles about B3PYMPM 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: bis-triphenylphosphine-palladium(II) chloride; sodium carbonate / water; acetonitrile / 6 h / 60 °C / Inert atmosphere
2: tris-(dibenzylideneacetone)dipalladium(0); potassium phosphate; tricyclohexylphosphine / 1,4-dioxane; water / 30 h / Inert atmosphere; Reflux
With bis-triphenylphosphine-palladium(II) chloride; potassium phosphate; tris-(dibenzylideneacetone)dipalladium(0); sodium carbonate; tricyclohexylphosphine; In 1,4-dioxane; water; acetonitrile; 1: Suzuki-Miyaura coupling reaction / 2: Suzuki-Miyaura coupling reaction;
DOI:10.1002/adfm.201001252
Guidance literature:
Multi-step reaction with 2 steps
1: bis-triphenylphosphine-palladium(II) chloride; sodium carbonate / water; acetonitrile / 6 h / 60 °C / Inert atmosphere
2: tris-(dibenzylideneacetone)dipalladium(0); potassium phosphate; tricyclohexylphosphine / 1,4-dioxane; water / 30 h / Inert atmosphere; Reflux
With bis-triphenylphosphine-palladium(II) chloride; potassium phosphate; tris-(dibenzylideneacetone)dipalladium(0); sodium carbonate; tricyclohexylphosphine; In 1,4-dioxane; water; acetonitrile; 1: Suzuki-Miyaura coupling reaction / 2: Suzuki-Miyaura coupling reaction;
DOI:10.1002/adfm.201001252
Guidance literature:
With potassium phosphate; tris-(dibenzylideneacetone)dipalladium(0); tricyclohexylphosphine; In 1,4-dioxane; water; for 24h; Inert atmosphere; Reflux;
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