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PHENYLMETHYLDICHLOROSILANE
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PHENYLMETHYLDICHLOROSILANE

CAS: 149-74-6

Ref. 3H-SIP6738.0

18kgA consultar
500gA consultar
200kgA consultar
Entrega estimada en Estados Unidos, el Martes 28 de Mayo de 2024

Información del producto

Nombre:
PHENYLMETHYLDICHLOROSILANE
Sinónimos:
  • (Dichloromethylsilyl)benzene
  • Benzene, (dichloromethylsilyl)-
  • Benzyl(Dichloro)Silane
  • Dichlor(methyl)(phenyl)silan
  • Dichloro(methyl)(phenyl)silane
  • Dichlorophenylmethylsilane
  • Dicloro(Fenil)(Metil)Silano
  • Ls 1490
  • Methylphenyldichlorosilane
  • Nsc 96621
  • Ver más sinónimos
  • Phenyldichloro(methyl)silane
  • Phenylmethyldichlorosilane
  • Silane, Methylphenyldichloro-
  • Silane, dichloromethylphenyl-
  • Tsl 8067
  • [(Dichloro)methylsilyl]benzene
Descripción:

Aromatic Silane - Conventional Surface Bonding
Aliphatic, fluorinated aliphatic or substituted aromatic hydrocarbon substituents are the hydrophobic entities which enable silanes to induce surface hydrophobicity. The organic substitution of the silane must be non-polar. The hydrophobic effect of the organic substitution can be related to the free energy of transfer of hydrocarbon molecules from an aqueous phase to a homogeneous hydrocarbon phase. A successful hydrophobic coating must eliminate or mitigate hydrogen bonding and shield polar surfaces from interaction with water by creating a non-polar interphase. Although silane and silicone derived coatings are in general the most hydrophobic, they maintain a high degree of permeability to water vapor. This allows coatings to breathe and reduce deterioration at the coating interface associated with entrapped water. Since ions are not transported through non-polar silane and silicone coatings, they offer protection to composite structures ranging from pigmented coatings to rebar reinforced concrete. A selection guide for hydrophobic silanes can be found on pages 22-31 of the Hydrophobicity, Hydrophilicity and Silane Surface Modification brochure.
Arylsilane Cross-Coupling Agent
The cross-coupling reaction is a highly useful methodology for the formation of carbon-carbon bonds. It involves two reagents, with one typically being a suitable organometallic reagent - the nucleophile - and the other a suitable organic substrate, normally an unsaturated halide, tosylate or similar - the electrophile.
Phenylmethyldichlorosilane; Methylphenyldichlorosilane; Dichloromethylphenylsilane
Viscosity, 20 °C: 1.2 cStΔHvap: 48.1 kJ/molVapor pressure, 82.5 °C: 13 mmMonomer for high temperature siliconesReacts well under the influence of NaOH versus fluoride activation w/ aryl chlorides, bromides, and iodides

Marca:
Gelest
Almacenamiento de larga duración:
Notas:

Propiedades químicas

Peso molecular:
191.13
Fórmula:
C7H8Cl2Si
Pureza:
97%
Color/Forma:
Liquid
MDL:
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Información de peligrosidad

Número UN:
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Consulta técnica sobre: 3H-SIP6738.0 PHENYLMETHYLDICHLOROSILANE

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