CAS 940-41-0

[2-(Triclorosilil)etil]benceno

Descripción:

[2-(Triclorosilil)etil]benceno, con el número CAS 940-41-0, es un compuesto organosilícico caracterizado por la presencia de un grupo tricloro-sililo unido a una cadena etílica, que a su vez está conectada a un anillo de benceno. Este compuesto típicamente aparece como un líquido incoloro a amarillo pálido y es conocido por su reactividad debido a la presencia del grupo funcional tricloro-sililo, que puede hidrolizarse fácilmente en presencia de humedad, liberando ácido clorhídrico y formando especies de silanol. Su estructura confiere propiedades tanto hidrofóbicas como lipofílicas, lo que lo hace útil en diversas aplicaciones, incluyendo como agente de acoplamiento en la química de polímeros y como precursor en la síntesis de materiales de silicona. Además, la reactividad del compuesto le permite participar en reacciones de entrecruzamiento, mejorando las propiedades mecánicas de los materiales. Se deben observar precauciones de seguridad al manipular esta sustancia, ya que puede ser corrosiva y perjudicial al contacto.

Fórmula: C₈H₉Cl₃Si

InChI: InChI=1S/C8H9Cl3Si/c9-12(10,11)7-6-8-4-2-1-3-5-8/h1-5H,6-7H2

Clave InChI: InChIKey=FMYXZXAKZWIOHO-UHFFFAOYSA-N

SMILES: C(C[Si](Cl)(Cl)Cl)C1=CC=CC=C1

Sinónimos:

• (2-Phenethyl)-trichlorosilane
• (2-Phenylethyl)trichlorosilane
• 1-(Trichlorosilyl)-2-phenylethane
• 1-Phenyl-2-(trichlorosilyl)ethane
• 2-(Trichlorosilyl)ethylbenzene
• 3-Phenethyltrichlorosilane
• Benzene, [2-(trichlorosilyl)ethyl]-
• Lp 1990
• NSC 139848
• Silane, trichloro(2-phenylethyl)-
• Silane, trichlorophenethyl-
• Trichloro(2-Phenylethyl)Silane
• Trichloro(phenethyl)silane
• Trichloro(phenylethyl)silane
• Trichloro(β-phenylethyl)silane
• Trichlorophenethylsilane
• [2-(Trichlorosilyl)ethyl]benzene

Trichloro(phenylethyl)silane (mixture of isomers)

CAS: 7726-28-5, 940-41-0

Fórmula: C₈H₉Cl₃Si

Pureza: >98.0%(GC)

Forma y color: Colorless to Light yellow to Light orange clear liquid

Peso molecular: 239.60

Ref: 3B-T2852

Trichloro(Phenethyl)Silane

CAS: 940-41-0

Trichloro(Phenethyl)Silane

Pureza: 97%

Peso molecular: 239.60g/mol

Ref: 54-OR1015309

PHENETHYLTRICHLOROSILANE

CAS: 940-41-0

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.
Phenethyltrichlorosilane; 2-(Trichlorosilylethyl) benzene; Trichloro(2-phenylethyl)silane
Contains α-, β-isomersTreated surface contact angle, water: 88°

Fórmula: C₈H₉Cl₃Si

Pureza: 97%

Forma y color: Pale Yellow Liquid

Peso molecular: 239.6

Ref: 3H-SIP6722.0

Phenethyltrichlorosilane

CAS: 940-41-0

S13200 - Phenethyltrichlorosilane

Fórmula: C₈H₉Cl₃Si

Pureza: 95%

Forma y color: Liquid, Clear

Peso molecular: 239.6

Ref: 10-S13200