32328-67-9 Usage
Uses
Used in Chemical Synthesis:
4-Phenylbutyldimethylchlorosilane is used as a reagent in the synthesis of organic and inorganic compounds, leveraging its unique structure to facilitate various chemical reactions.
Used in Silicone Polymer Production:
4-PHENYLBUTYLDIMETHYLCHLOROSILANE serves as a key ingredient in the production of silicone polymers, which are known for their heat resistance, flexibility, and biocompatibility.
Used in Surface Modification:
4-Phenylbutyldimethylchlorosilane is used as a surface modifier to alter the properties of materials, such as enhancing their water-repellency and hydrophobicity, which is beneficial in applications requiring non-stick or easy-to-clean surfaces.
Used in Adhesive and Sealant Formulation:
As a crosslinking agent, 4-Phenylbutyldimethylchlorosilane is incorporated into the formulation of adhesives and sealants to improve their bonding strength and durability.
Used in Specialty Chemical Production:
4-PHENYLBUTYLDIMETHYLCHLOROSILANE acts as a precursor in the production of specialty chemicals, contributing to the development of unique products with specific applications in various industries.
Used in Industrial Applications:
4-Phenylbutyldimethylchlorosilane is utilized in a variety of industrial applications due to its water-repellent and hydrophobic properties, making it suitable for creating protective coatings and improving material performance in diverse settings.
Check Digit Verification of cas no
The CAS Registry Mumber 32328-67-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,2 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 32328-67:
(7*3)+(6*2)+(5*3)+(4*2)+(3*8)+(2*6)+(1*7)=99
99 % 10 = 9
So 32328-67-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H19ClSi/c1-14(2,13)11-7-6-10-12-8-4-3-5-9-12/h3-5,8-9H,6-7,10-11H2,1-2H3
32328-67-9Relevant academic research and scientific papers
RINGOEFFNUNG UND METALLIERUNG VON 1,1-DIMETHYL-2-PHENYL-SILACYCLOPENTAN UNTER DEM EINFLUSS VON METHYLLITHIUM IN TETRAHYDROFURAN
Maercker, Adalbert,Stoetzel, Reinhard
, p. C40 - C46 (2007/10/02)
In contrast to 1-phenylethyllithium, which reacts as a base, methyllithium attacks the silicon atom of 1,1-dimethyl-2-phenyl-silacyclopentane (7) as a nucleophile whereby ring-opening takes place presumably via an ate-complex intermediate.The primarily fo
