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Silane, trimethyl(4-nitrophenyl)-

Base Information
  • Chemical Name:Silane, trimethyl(4-nitrophenyl)-
  • CAS No.:4405-33-8
  • Molecular Formula:C9H13 N O2 Si
  • Molecular Weight:195.293
  • Hs Code.:2931900090
  • DSSTox Substance ID:DTXSID50196028
  • Nikkaji Number:J46.918A
  • Wikidata:Q63408862
  • Mol file:4405-33-8.mol
Silane, trimethyl(4-nitrophenyl)-

Synonyms:4405-33-8;Silane, trimethyl(4-nitrophenyl)-;trimethyl-(4-nitrophenyl)silane;(4-Nitrophenyl)trimethylsilane;p-Nitrophenyltrimethylsilane;Silane,trimethyl(4-nitrophenyl)-;4-(Trimethylsilyl)-1-nitrobenzene;SCHEMBL4927395;DTXSID50196028;PARA-NITROPHENYLTRIMETHYLSILANE;TRIMETHYL(4-NITROPHENYL)SILANE;AKOS024338487;Q63408862

Suppliers and Price of Silane, trimethyl(4-nitrophenyl)-
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
  • Packaging
  • price
  • Sigma-Aldrich
  • (4-NITROPHENYL)TRIMETHYLSILANE Aldrich
  • 50mg
  • $ 144.00
  • American Custom Chemicals Corporation
  • (4-NITROPHENYL)TRIMETHYLSILANE 95.00%
  • 1G
  • $ 827.40
Total 3 raw suppliers
Chemical Property of Silane, trimethyl(4-nitrophenyl)-
Chemical Property:
  • Vapor Pressure:0.0226mmHg at 25°C 
  • Boiling Point:258.1°C at 760 mmHg 
  • Flash Point:109.9°C 
  • PSA:45.82000 
  • Density:1.04g/cm3 
  • LogP:2.66320 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:1
  • Exact Mass:195.071555192
  • Heavy Atom Count:13
  • Complexity:187
Purity/Quality:

(4-NITROPHENYL)TRIMETHYLSILANE Aldrich *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C[Si](C)(C)C1=CC=C(C=C1)[N+](=O)[O-]
  • General Description 1-(Trimethylsilyl)-4-nitrobenzene is a nitro-substituted aromatic silane compound characterized by a trimethylsilyl group attached to the para position of a nitrobenzene ring. The presence of the nitro group induces intramolecular charge transfer, leading to significant red shifts in UV spectra compared to non-nitro-substituted analogs, as observed in related nitrophenylpolysilanes. While the provided abstracts do not directly describe its synthesis or properties, the compound shares structural and electronic similarities with other nitrophenylsilane derivatives, suggesting potential applications in materials or synthetic chemistry due to its electron-withdrawing nitro group and silyl functionality.
Technology Process of Silane, trimethyl(4-nitrophenyl)-

There total 15 articles about Silane, trimethyl(4-nitrophenyl)- 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 water; tris-(dibenzylideneacetone)dipalladium(0); In N,N-dimethyl-formamide; at 100 ℃; for 24h;
DOI:10.1021/ol701518f
Guidance literature:
With nitric acid; at 80 - 100 ℃; Acidic conditions;
DOI:10.1039/d1cc06497e
Guidance literature:
With MePhos Pd G4; In 1,2-dichloro-ethane; at 50 ℃;
DOI:10.1021/acscatal.1c02733
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