18147-23-4 Usage
Uses
Used in Chemical Industry:
N-BUTYLMETHYLDICHLOROSILANE is used as a coupling agent and a precursor for the synthesis of organosilicon compounds and coatings. Its role in this industry is crucial for enhancing the properties of materials and creating new applications for various products.
Used in Manufacturing of Adhesion Promoters, Sealants, and Adhesives:
N-BUTYLMETHYLDICHLOROSILANE is used as a reactive intermediate in the production of these products, improving their bonding capabilities and performance in various applications.
Used in Waterproofing and Protective Coatings:
Leveraging its water-repellent properties, N-BUTYLMETHYLDICHLOROSILANE is used as a key ingredient in the formulation of waterproofing agents and protective coatings for a range of surfaces, providing enhanced durability and resistance to environmental factors.
Overall, N-BUTYLMETHYLDICHLOROSILANE's applications span across multiple industries, highlighting its importance in the development and improvement of various products and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 18147-23-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,4 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18147-23:
(7*1)+(6*8)+(5*1)+(4*4)+(3*7)+(2*2)+(1*3)=104
104 % 10 = 4
So 18147-23-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H12Cl2Si/c1-3-4-5-8(2,6)7/h3-5H2,1-2H3
18147-23-4Relevant academic research and scientific papers
Quantitative substituent effects in the Grignard reaction with silanes
Golubev, Oleg,Panov, Dmitri,Ploom, Anu,Tuulmets, Ants,Nguyen, Binh T.
, p. 3700 - 3705 (2008/02/08)
Kinetics of reactions of ethyl- and phenylmagnesium chlorides with chlorosilanes, RMeSiCl2, were investigated in diethyl ether under pseudo-first order conditions with a great excess of the Grignard reagent. Rate constants for alkyl substituted silanes correlate well with Es(Si) steric parameters. A good linear correlation of rate data for substituted phenyl derivates with σ0 inductive constants together with correlations of the literature data rule out the resonance effect of substituents at least in nucleophilic displacement reactions at the silicon center. An attempt to calculate the steric constants for polar substituents was made. It appeared that the inductive constants σ* derived from the carbon chemistry are not applicable to the silicon chemistry. New scales of parameters for description of polar and steric effects in the organosilicon chemistry need to be created.
