18028-96-1 Usage
Uses
Used in Organic Synthesis:
DICHLOROISOBUTYLMETHYLSILANE is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, facilitating the creation of a range of organic compounds.
Used in Silicone-based Chemical Production:
DICHLOROISOBUTYLMETHYLSILANE is used as a building block in the production of other silicone-based chemicals, contributing to the development of materials with diverse applications across different industries.
Used in Chemical Research:
In the field of chemical research, DICHLOROISOBUTYLMETHYLSILANE is utilized as a subject of study to explore its reactivity and potential applications in advancing chemical processes and material science.
Used in Pharmaceutical Industry:
DICHLOROISOBUTYLMETHYLSILANE may be used as an intermediate in the synthesis of pharmaceutical compounds, given its reactivity and the ability to form new chemical entities with potential therapeutic properties.
Used in Material Science:
In material science, DICHLOROISOBUTYLMETHYLSILANE is used as a component in the development of new materials, potentially enhancing the properties of existing materials or creating novel materials with unique characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 18028-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,2 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18028-96:
(7*1)+(6*8)+(5*0)+(4*2)+(3*8)+(2*9)+(1*6)=111
111 % 10 = 1
So 18028-96-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H12Cl2Si/c1-5(2)4-8(3,6)7/h5H,4H2,1-3H3
18028-96-1Relevant 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.
