CAS 780-69-8

Feniltrietoxisilano

Descripción:

Feniltrietoxisilano, con el número CAS 780-69-8, es un compuesto organosilícico caracterizado por su estructura de silano, que incluye un grupo fenilo y tres grupos etóxido unidos a un átomo de silicio. Este compuesto es típicamente un líquido incoloro a amarillo pálido y es conocido por su capacidad para unirse tanto a materiales orgánicos como inorgánicos, lo que lo hace útil como agente de acoplamiento y modificador de superficie. Exhibe buena estabilidad térmica y propiedades hidrofóbicas, lo que mejora su aplicabilidad en diversas formulaciones, incluyendo recubrimientos, adhesivos y selladores. Además, Feniltrietoxisilano puede mejorar la adhesión de polímeros orgánicos a sustratos inorgánicos, como vidrio y metales, debido a su funcionalidad de silano. Su reactividad le permite someterse a hidrólisis en presencia de humedad, lo que lleva a la formación de grupos silanol que pueden polimerizarse o unirse a superficies. En general, este compuesto es valorado en industrias como la construcción, la electrónica y la ciencia de materiales por su versatilidad y efectividad en la mejora de las propiedades de los materiales.

Fórmula: C₁₂H₂₀O₃Si

InChI: InChI=1S/C12H20O3Si/c1-4-13-16(14-5-2,15-6-3)12-10-8-7-9-11-12/h7-11H,4-6H2,1-3H3

Clave InChI: InChIKey=JCVQKRGIASEUKR-UHFFFAOYSA-N

SMILES: [Si](OCC)(OCC)(OCC)C1=CC=CC=C1

Sinónimos:

• (Triethoxysilyl)benzene
• Benzene, (triethoxysilyl)-
• Benzeneorthosiliconic acid, triethyl ester
• Dynasil 9265
• Dynasylan 9265
• Kbe 103
• Kbm 202Ls4480
• Kh 162
• Kh 651
• Ls 4480
• Ls 4800
• Nsc 77115
• P 0320
• Phenyltriethoxysilane
• Pts 32
• Sip 6821.0
• Tri(ethoxo)(phenyl)silane
• Triethoxy(phenyl)silan
• Triethoxy(phenyl)silane
• Triethoxyphenylsilane
• Trietoxi(Fenil)Silano
• Tsl 8178

Triethoxyphenylsilane

CAS: 780-69-8

Fórmula: C₁₂H₂₀O₃Si

Pureza: >99.0%(GC)

Forma y color: Colorless to Almost colorless clear liquid

Peso molecular: 240.37

Ref: 3B-P0735

Phenyltriethoxysilane, 98%

CAS: 780-69-8

Phenyltriethoxysilane is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff fields. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may ref

Fórmula: C₁₂H₂₀O₃Si

Pureza: 98%

Forma y color: Clear colorless, Liquid or viscous liquid

Peso molecular: 240.37

Ref: 02-L04684

Phenyltriethoxysilane

CAS: 780-69-8

Phenyltriethoxysilane

Pureza: 98%

Peso molecular: 240.37g/mol

Ref: 54-OR1014658

Phenyltriethoxysilane

CAS: 780-69-8

S13700 - Phenyltriethoxysilane

Fórmula: C₁₂H₂₀O₃Si

Pureza: 95%

Forma y color: Liquid, Colourless liquid

Peso molecular: 240.374

Ref: 10-S13700

PHENYLTRIETHOXYSILANE

CAS: 780-69-8

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.
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.
Phenyltriethoxysilane; Triethoxysilylbenzene; Triethoxy(phenyl)silane
Viscosity, 25 °C: 1.7 cStDipole moment: 1.85 debyeSurface tension: 28 mN/mDielectric constant: 4.12Vapor pressure, 75 °C: 1 mmCoefficient of thermal expansion: 0.9 x 10-3Improves photoresist adhesion to silicon nitrideElectron donor component of polyolefin polymerization catalyst complexesEffective treatment for organic-grafted claysPhenylates allyl benzoatesCross-couples with aryl bromides without amine or phosphineligandsPhenylates allyl acetatesβ-phenylates enones under aqueous base conditionsExtensive review of silicon based cross-coupling agents: Denmark, S. E. et al. "Organic Reactions, Volume 75"Denmark, S. E. ed., John Wiley and Sons, 233, 2011

Fórmula: C₁₂H₂₀O₃Si

Pureza: 97%

Forma y color: Straw Liquid

Peso molecular: 240.37

Ref: 3H-SIP6821.0