Trimethyl-p-tolylsilane, 95%
Trimethyl-p-tolylsilane, 95%
Trimethyl-p-tolylsilane, 95%
Thermo Scientific Chemicals

Trimethyl-p-tolylsilane, 95%

CAS: 3728-43-6 | C10H16Si | 164.323 g/mol
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Quantity:
5 g
25 g
Catalog number A17884.06
also known as A17884-06
Price (EUR)
91,10
Each
Quantity:
5 g
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Price (EUR)
91,10
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Chemical Identifiers
CAS3728-43-6
IUPAC Nametrimethyl(4-methylphenyl)silane
Molecular FormulaC10H16Si
InChI KeyQGHURGPPCGMAMZ-UHFFFAOYSA-N
SMILESCC1=CC=C(C=C1)[Si](C)(C)C
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless
Assay (GC)≥96.0%
Refractive Index1.4885-1.4935 @ 20?C
FormLiquid
It is employed in the production of trimethyl-(4-trimethylsilanyl-benzyl)-silane by reacting with chloro-trimethyl-silane.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
It is employed in the production of trimethyl-(4-trimethylsilanyl-benzyl)-silane by reacting with chloro-trimethyl-silane.

Solubility
Not miscible or difficult to mix in water.

Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition. Protect against electrostatic charges. Keep ignition sources away.
RUO – Research Use Only

General References:

  1. Dr. Guy Félix.; Dr. Jacques Dunoguès.; Dr. Francoise Pisciotti and Prof. Raymond Calas. Regiospecific Synthesis of Mono-and Polyiodo Derivatives of Benzene.Angew. Chem. Int. Ed.,1977,16(7), 488-489.
  2. Tetsutaro Hattori.; Yutaka Suzuki.; Sotaro Miyano. Lewis Acid-Mediated Carboxylation of Aryl- and Allylsilanes with Carbon Dioxide.Chem. Lett.,2003,23(5 P), 454-455.