Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

1-Methyl-4,5-diphenyl-4,5-dihydro-1H-tetrazaborole

Base Information Edit
  • Chemical Name:1-Methyl-4,5-diphenyl-4,5-dihydro-1H-tetrazaborole
  • CAS No.:114027-14-4
  • Molecular Formula:C13H13BN4
  • Molecular Weight:236.084
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40549509
  • Wikidata:Q82428577
  • Mol file:114027-14-4.mol
1-Methyl-4,5-diphenyl-4,5-dihydro-1H-tetrazaborole

Synonyms:114027-14-4;1-Methyl-4,5-diphenyl-4,5-dihydro-1H-tetrazaborole;DTXSID40549509

Suppliers and Price of 1-Methyl-4,5-diphenyl-4,5-dihydro-1H-tetrazaborole
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
Total 1 raw suppliers
Chemical Property of 1-Methyl-4,5-diphenyl-4,5-dihydro-1H-tetrazaborole Edit
Chemical Property:
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:2
  • Exact Mass:236.1233266
  • Heavy Atom Count:18
  • Complexity:297
Purity/Quality:

99.90% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:B1(N(N=NN1C2=CC=CC=C2)C)C3=CC=CC=C3
Technology Process of 1-Methyl-4,5-diphenyl-4,5-dihydro-1H-tetrazaborole

There total 1 articles about 1-Methyl-4,5-diphenyl-4,5-dihydro-1H-tetrazaborole 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 dichloromethane; soln. of azide and of N-trimethylsilylamino-chloroborane in CH2Cl2 is stirred at 40°C for 8 h (under N2); removal of the solvent provided an oily residue which is purified by column chromy. (silica gel, ether/hexane), elem. anal.;
DOI:10.1016/0022-328X(87)80222-X
Post RFQ for Price