Benzenamine, 2,5-bis[[(1,1-dimethylethyl)dimethylsilyl]oxy]-

Base Information

Chemical Name:Benzenamine, 2,5-bis[[(1,1-dimethylethyl)dimethylsilyl]oxy]-
CAS No.:159898-39-2
Molecular Formula:C18H35NO2Si2
Molecular Weight:353.652
Hs Code.:
DSSTox Substance ID:DTXSID20447019
Wikidata:Q82265795
Mol file:159898-39-2.mol

Synonyms:Benzenamine, 2,5-bis[[(1,1-dimethylethyl)dimethylsilyl]oxy]-;159898-39-2;DTXSID20447019

Suppliers and Price of Benzenamine, 2,5-bis[[(1,1-dimethylethyl)dimethylsilyl]oxy]-

Supply Marketing:

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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price

Total 1 raw suppliers

Chemical Property of Benzenamine, 2,5-bis[[(1,1-dimethylethyl)dimethylsilyl]oxy]-

Chemical Property:

Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:353.22063243
Heavy Atom Count:23
Complexity:397

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)[Si](C)(C)OC1=CC(=C(C=C1)O[Si](C)(C)C(C)(C)C)N

Technology Process of Benzenamine, 2,5-bis[[(1,1-dimethylethyl)dimethylsilyl]oxy]-

There total 6 articles about Benzenamine, 2,5-bis[[(1,1-dimethylethyl)dimethylsilyl]oxy]- 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: 83.0%

: 159898-38-1
1,4-Bis-(tert-butyl-dimethyl-silanyloxy)-2-nitro-benzene

: 159898-39-2
2-amino-1,4-<(tert-butyldimethylsilyl)oxy>benzene

Guidance literature:: With sodium tetrahydroborate; nickel dichloride; In methanol; Ambient temperature;
DOI:10.1016/0040-4039(94)88253-3

Reference yield: 80.0%

: 185330-19-2
2-Azido-1,4-bis-(tert-butyl-dimethyl-silanyloxy)-benzene

: 159898-39-2
2-amino-1,4-<(tert-butyldimethylsilyl)oxy>benzene

Guidance literature:: With sodium tetrahydroborate; nickel dichloride; In methanol; at 0 ℃; for 0.25h;
DOI:10.1021/jo9614708

Reference yield:

: 185330-16-9
2‐azidobenzene‐1,4‐diol

: 159898-39-2
2-amino-1,4-<(tert-butyldimethylsilyl)oxy>benzene

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / imidazole / dimethylformamide / 2 h / Ambient temperature

2: 80 percent / NaBH₄, NiCl₂*6H₂O / methanol / 0.25 h / 0 °C

With 1H-imidazole; sodium tetrahydroborate; nickel dichloride; In methanol; N,N-dimethyl-formamide;
DOI:10.1021/jo9614708