CAS 37843-11-1

1-[2-(Trichlorosilyl)ethyl]tricyclo[3.3.1.13,7]decane

Description:

1-[2-(Trichlorosilyl)ethyl]tricyclo[3.3.1.13,7]decane, with the CAS number 37843-11-1, is a chemical compound characterized by its unique structure that combines a tricyclic hydrocarbon framework with a trichlorosilyl functional group. The presence of the trichlorosilyl group indicates that this compound may exhibit reactivity typical of organosilicon compounds, particularly in terms of its potential to participate in reactions involving silicon and chlorine functionalities. The tricyclo[3.3.1.13,7]decane structure contributes to its rigidity and may influence its physical properties, such as boiling point and solubility. Additionally, the compound may display interesting chemical behavior due to the steric and electronic effects of the trichlorosilyl group, which can affect its reactivity and interactions with other substances. Overall, this compound is of interest in various fields, including materials science and organic synthesis, due to its unique structural features and potential applications in creating silicon-containing materials.

Formula: C₁₂H₁₉Cl₃Si

InChI: InChI=1S/C12H19Cl3Si/c13-16(14,15)2-1-12-6-9-3-10(7-12)5-11(4-9)8-12/h9-11H,1-8H2

InChI key: InChIKey=HLBWWITUVOEXHH-UHFFFAOYSA-N

SMILES: C(C[Si](Cl)(Cl)Cl)C12CC3CC(C1)CC(C2)C3

Synonyms:

• 1-[2-(Trichlorosilyl)ethyl]adamantane
• 1-[2-(Trichlorosilyl)ethyl]tricyclo[3.3.1.1^3,7]decane
• 2-(1-Adamantyl)ethyltrichlorosilane
• Silane, trichloro(2-tricyclo(3.3.1.13,7)dec-1-ylethyl)-
• Silane, trichloro(2-tricyclo[3.3.1.1^3,7]dec-1-ylethyl)-
• Trichloro(2-tricyclo(3.3.1.13,7)decylethyl)silane
• Trichloro[2-(Tricyclo[3.3.1.1~3,7~]Dec-1-Yl)Ethyl]Silane
• Tricyclo(3.3.1.13,7)decane, 1-(2-(trichlorosilyl)ethyl)-
• Tricyclo[3.3.1.1^3,7]decane, 1-[2-(trichlorosilyl)ethyl]-
• 1-[2-(Trichlorosilyl)ethyl]tricyclo[3.3.1.13,7]decane

ADAMANTYLETHYLTRICHLOROSILANE

CAS: 37843-11-1

Alkyl 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.
Adamantylethyltrichlorosilane; Trichlorosilylethyladamantane; Trichloro(2-tricyclo[3.3.1.13,7]decylethyl)silane
Contains approximately 25% α-isomerForms silica bonded phases for reverse phase chromatography

Formula: C₁₂H₁₉Cl₃Si

Purity: 97%

Color and Shape: Off-White Solid

Molecular weight: 297.73

Ref: 3H-SIA0325.0