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Benzenecarboximidic acid, N-[(trimethylsilyl)oxy]-, trimethylsilyl ester

Base Information Edit
  • Chemical Name:Benzenecarboximidic acid, N-[(trimethylsilyl)oxy]-, trimethylsilyl ester
  • CAS No.:77219-88-6
  • Molecular Formula:C13H23NO2Si2
  • Molecular Weight:281.502
  • Hs Code.:
  • DSSTox Substance ID:DTXSID70396184
  • Mol file:77219-88-6.mol
Benzenecarboximidic acid, N-[(trimethylsilyl)oxy]-, trimethylsilyl ester

Synonyms:Benzenecarboximidic acid, N-[(trimethylsilyl)oxy]-, trimethylsilyl ester;77219-88-6;DTXSID70396184

Suppliers and Price of Benzenecarboximidic acid, N-[(trimethylsilyl)oxy]-, trimethylsilyl ester
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
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Total 0 raw suppliers
Chemical Property of Benzenecarboximidic acid, N-[(trimethylsilyl)oxy]-, trimethylsilyl ester Edit
Chemical Property:
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:5
  • Exact Mass:281.12673205
  • Heavy Atom Count:18
  • Complexity:286
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C[Si](C)(C)OC(=NO[Si](C)(C)C)C1=CC=CC=C1
Technology Process of Benzenecarboximidic acid, N-[(trimethylsilyl)oxy]-, trimethylsilyl ester

There total 2 articles about Benzenecarboximidic acid, N-[(trimethylsilyl)oxy]-, trimethylsilyl ester 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 triethylamine; In tetrahydrofuran; at 22 ℃; for 4h; Yield given;
Guidance literature:
at 100 ℃; for 1.5h;
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