CAS 67373-56-2
:Thexyldimethylchlorosilane
Description:
Thexyldimethylchlorosilane, with the CAS number 67373-56-2, is an organosilicon compound characterized by its chlorosilane functional group. It typically appears as a colorless to pale yellow liquid with a distinctive odor. This compound is known for its reactivity, particularly in hydrolysis, where it can react with water to produce silanol and hydrochloric acid. Thexyldimethylchlorosilane is utilized primarily in the synthesis of silicone polymers and as a coupling agent in various chemical processes. Its structure includes a silicon atom bonded to two methyl groups and one hexyl group, along with a chlorine atom, which contributes to its unique properties. The presence of the hexyl group enhances its hydrophobic characteristics, making it useful in applications requiring water repellency. Safety precautions are necessary when handling this substance, as it can be corrosive and may pose health risks if inhaled or ingested. Proper storage in a cool, dry place away from moisture is essential to maintain its stability and effectiveness in industrial applications.
Formula:C8H19ClSi
InChI:InChI=1/C8H19ClSi/c1-7(2)8(3,4)10(5,6)9/h7H,1-6H3
SMILES:CC(C)C(C)(C)[Si](C)(C)Cl
Synonyms:- Dimethylthexylsilyl chloride
- Chloro(2,3-Dimethylbutan-2-Yl)Dimethylsilane
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Found 4 products.
Chloro(dimethyl)thexylsilane
CAS:Formula:C8H19ClSiPurity:>95.0%(GC)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:178.78DIMETHYLTHEXYLSILYL CHLORIDE
CAS:Formula:C8H19ClSiPurity:95%Color and Shape:LiquidMolecular weight:178.7750THEXYLDIMETHYLCHLOROSILANE
CAS:<p>Alkyl Silane - Conventional Surface Bonding<br>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.<br>Trialkylsilyl Blocking Agent<br>Used as a protecting group for reactive hydrogens in alcohols, amines, thiols, and carboxylic acids. Organosilanes are hydrogen-like, can be introduced in high yield, and can be removed under selective conditions. They are stable over a wide range of reaction conditions and can be removed in the presence of other functional groups, including other protecting groups. The tolerance of silylated alcohols to chemical transformations summary is presented in Table 1 of the Silicon-Based Blocking Agents brochure.<br>Thexyldimethylchlorosilane; t-Hexyldimethylchlorosilane; Dimethylthexylchlorosilane; TDS-Cl<br>Ethers show stability similar to or greater than the TBS ethers.Used for 1° and 2° aminesSelective for 1° alcoholsHighly stable protection of alcohols, amines, amides, mercaptans and acidsThe N-silylated β-lactam shows increased hydrolytic stability over that of the analogous N-TBS derivativeSummary of selective deprotection conditions is provided in Table 7 through Table 20 of the Silicon-Based Blocking Agents brochure<br></p>Formula:C8H19ClSiPurity:97%Color and Shape:LiquidMolecular weight:178.78
