CAS 68128-25-6

1-(Chloromethyl)-3(or 4)-[2-(trimethoxysilyl)ethyl]benzene

Description:

1-(Chloromethyl)-3(or 4)-[2-(trimethoxysilyl)ethyl]benzene, with the CAS number 68128-25-6, is an organosilicon compound characterized by the presence of both a chloromethyl group and a trimethoxysilyl group attached to a benzene ring. This compound typically exhibits properties associated with both organic and inorganic chemistry due to its hybrid structure. The chloromethyl group can participate in nucleophilic substitution reactions, making it a useful intermediate in organic synthesis. The trimethoxysilyl group enhances the compound's ability to bond with silicate materials, promoting adhesion and compatibility with various substrates, which is particularly valuable in coatings and sealants. Additionally, the presence of the aromatic benzene ring contributes to the compound's stability and hydrophobic characteristics. Overall, this compound is of interest in materials science and surface chemistry, particularly for applications involving silane coupling agents and functionalization of surfaces.

Formula: C₁₂H₁₉ClO₃Si

InChI: InChI=1/C12H19ClO3Si/c1-14-17(15-2,16-3)9-8-11-4-6-12(10-13)7-5-11/h4-7H,8-10H2,1-3H3

SMILES: CO[Si](CCc1ccc(cc1)CCl)(OC)OC

Synonyms:

• (2-(3(Or4)-(chloromethyl)phenyl)ethyl)trimethoxysilane
• 1-(Chloromethyl)-3(or 4)-[2-(trimethoxysilyl)ethyl]benzene
• 1-Trimethoxysilyl-2-(m,p-chloromethyl)phenylethane
• 1-Trimethoxysilyl-2-(p,m-chloromethyl)phenylethane
• 2-(m/p-Chloromethylphenyl)ethyltrimethoxysilane
• Benzene, 1-(chloromethyl)-3(or 4)-(2-(trimethoxysilyl)ethyl)-
• Silane, (2-(3(or 4)-(chloromethyl)phenyl)ethyl)trimethoxy-
• {2-[4-(Chloromethyl)Phenyl]Ethyl}(Trimethoxy)Silane

((CHLOROMETHYL)PHENYLETHYL)TRIMETHOXYSILANE

CAS: 68128-25-6

Halogen Functional Trialkoxy Silane
Silane coupling agents have the ability to form a durable bond between organic and inorganic materials to generate desired heterogeneous environments or to incorporate the bulk properties of different phases into a uniform composite structure. The general formula has two classes of functionality. The hydrolyzable group forms stable condensation products with siliceous surfaces and other oxides such as those of aluminum, zirconium, tin, titanium, and nickel. The organofunctional group alters the wetting or adhesion characteristics of the substrate, utilizes the substrate to catalyze chemical transformations at the heterogeneous interface, orders the interfacial region, or modifies its partition characteristics, and significantly effects the covalent bond between organic and inorganic materials.
((Chloromethyl)phenylethyl)trimethoxysilane; [2-[3(or 4)-(Chloromethyl)phenyl]ethyl]trimethoxysilane; (Trimethoxysilylethyl)benzyl chloride
Mixed m-, p- isomersUsed in microparticle surface modificationAdhesion promoter for polyphenylenesulfide and polyimide coatingsEmployed as a high temperature coupling agentDetermined by TGA a 25% weight loss of dried hydrolysates at 495 °CReagent for surface initiated atom-transfer radical-polymerization (ATRP) of N-isopropylacrylamide-butylmethacrylate copolymers

Formula: C₁₂H₁₉ClO₃Si

Purity: 97%

Color and Shape: Straw Liquid

Molecular weight: 274.82

Ref: 3H-SIC2295.5

((Chloromethyl)phenylethyl)trimethoxysilane

CAS: 68128-25-6

S25108 - ((Chloromethyl)phenylethyl)trimethoxysilane

Formula: C₁₂H₁₉ClO₃Si

Purity: 95%

Color and Shape: Liquid, Clear

Molecular weight: 274.82

Ref: 10-S25108