Silanamine, 1,1,1-triethyl-N-phenyl-N-(phenylmethyl)-

Base Information

Chemical Name:Silanamine, 1,1,1-triethyl-N-phenyl-N-(phenylmethyl)-
CAS No.:18641-46-8
Molecular Formula:C19H27NSi
Molecular Weight:297.516
Hs Code.:
DSSTox Substance ID:DTXSID80459214
Nikkaji Number:J3.072.638C
Wikidata:Q82282919

Synonyms:18641-46-8;Silanamine, 1,1,1-triethyl-N-phenyl-N-(phenylmethyl)-;DTXSID80459214;N-benzyl-N-(triethylsilyl)aniline;N-Phenyl-N-(triethylsilyl)benzylamine

Suppliers and Price of Silanamine, 1,1,1-triethyl-N-phenyl-N-(phenylmethyl)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Silanamine, 1,1,1-triethyl-N-phenyl-N-(phenylmethyl)-

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:7
Exact Mass:297.191276400
Heavy Atom Count:21
Complexity:267

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC[Si](CC)(CC)N(CC1=CC=CC=C1)C2=CC=CC=C2

Technology Process of Silanamine, 1,1,1-triethyl-N-phenyl-N-(phenylmethyl)-

There total 3 articles about Silanamine, 1,1,1-triethyl-N-phenyl-N-(phenylmethyl)- 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:

Reference yield:

: 617-86-7
triethylsilane

: 1750-36-3,33993-35-0,538-51-2,137431-97-1,137432-04-3
(E)-N-benzylidenebenzenamine

: 758640-21-0,103-32-2
N-Benzylaniline

: 18641-46-8
N-benzyl-1,1,1-triethyl-N-phenylsilanamine

Guidance literature:: With {Ir(bpm)(CO)2}BPh₄; In tetrahydrofuran-d8; at 60 ℃; for 24h;
DOI:10.1002/ejoc.200500168

Reference yield:

: 636-04-4
N-Phenylbenzothioamide

: 18641-46-8
N-benzyl-1,1,1-triethyl-N-phenylsilanamine

Guidance literature:: Multi-step reaction with 2 steps

1: dicarbonyl(cyclopentadienyl)methyliron(II); triethylsilane / tetrahydrofuran / 15 h / 80 °C / Inert atmosphere; Schlenk technique

2: dicarbonyl(cyclopentadienyl)methyliron(II) / benzene-d6 / 24 h / 80 °C / Sealed tube; Inert atmosphere

With triethylsilane; dicarbonyl(cyclopentadienyl)methyliron(II); In tetrahydrofuran; benzene-d6;
DOI:10.1002/hc.21175