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Borazine, 2,4,6-trichloro-1,3,5-triphenyl-

Base Information Edit
  • Chemical Name:Borazine, 2,4,6-trichloro-1,3,5-triphenyl-
  • CAS No.:981-87-3
  • Molecular Formula:C18H15 B3 Cl3 N3
  • Molecular Weight:412.129
  • Hs Code.:
  • DSSTox Substance ID:DTXSID90243444
  • Wikidata:Q83127532
  • Mol file:981-87-3.mol
Borazine, 2,4,6-trichloro-1,3,5-triphenyl-

Synonyms:BRN 2188485;BORAZINE, 2,4,6-TRICHLORO-1,3,5-TRIPHENYL-;DTXSID90243444;LS-45018

Suppliers and Price of Borazine, 2,4,6-trichloro-1,3,5-triphenyl-
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
  • 2,4,6-TRICHLORO-1,3,5-TRIPHENYLBORAZINE 95.00%
  • 5MG
  • $ 498.55
Total 5 raw suppliers
Chemical Property of Borazine, 2,4,6-trichloro-1,3,5-triphenyl- Edit
Chemical Property:
  • Vapor Pressure:2.05E-08mmHg at 25°C 
  • Boiling Point:453.5°Cat760mmHg 
  • Flash Point:228.1°C 
  • PSA:9.72000 
  • Density:1.32g/cm3 
  • LogP:2.36730 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:3
  • Exact Mass:411.061071
  • Heavy Atom Count:27
  • Complexity:389
Purity/Quality:

98%min *data from raw suppliers

2,4,6-TRICHLORO-1,3,5-TRIPHENYLBORAZINE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:B1(N(B(N(B(N1Cl)C2=CC=CC=C2)Cl)C3=CC=CC=C3)Cl)C4=CC=CC=C4
Technology Process of Borazine, 2,4,6-trichloro-1,3,5-triphenyl-

There total 11 articles about Borazine, 2,4,6-trichloro-1,3,5-triphenyl- 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:
In toluene; under dry aslow addn. of a soln. of organic compound to an ice-cooled soln. of BCl3, refluxing for 4 h; cooling, concg.;
DOI:10.1016/0022-328X(94)80079-0
Guidance literature:
With hydrogenchloride; benzene;
DOI:10.1021/ja01875a017
Guidance literature:
With triethylamine; In toluene;
DOI:10.1039/j19660000479
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