1072-54-4 Usage
Uses
Used in Silicone Rubber and Resin Manufacturing:
CYCLOTETRAMETHYLENEDIMETHYLSILANE is used as a silane coupling agent for enhancing the adhesion and bonding properties of silicone rubber and resins. Its incorporation into these materials results in improved performance characteristics, making it an essential component in their production.
Used in Adhesives and Sealants Production:
As a result of its bonding-enhancing properties, CYCLOTETRAMETHYLENEDIMETHYLSILANE is utilized as a critical ingredient in the formulation of adhesives and sealants. This application takes advantage of its ability to create strong bonds between various substrates, contributing to the effectiveness and durability of these products.
Used in Coatings Industry:
CYCLOTETRAMETHYLENEDIMETHYLSILANE is also used in the development of coatings that require robust adhesion and durability. CYCLOTETRAMETHYLENEDIMETHYLSILANE's role in this industry is to ensure that the coatings maintain a strong bond with the surfaces they are applied to, providing long-lasting protection and appearance.
Used in Specialty Silicones Synthesis:
CYCLOTETRAMETHYLENEDIMETHYLSILANE serves as a key building block in the synthesis of specialty silicones, which are tailored for specific applications that require unique properties, such as high temperature resistance or specific mechanical characteristics.
Used in Organosilicon Compounds Preparation:
Furthermore, the compound is utilized in the preparation of a variety of organosilicon compounds, which are important in numerous industrial applications due to their diverse and valuable properties, including their role in enhancing material performance and functionality.
Check Digit Verification of cas no
The CAS Registry Mumber 1072-54-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1072-54:
(6*1)+(5*0)+(4*7)+(3*2)+(2*5)+(1*4)=54
54 % 10 = 4
So 1072-54-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H14Si/c1-7(2)5-3-4-6-7/h3-6H2,1-2H3
1072-54-4Relevant academic research and scientific papers
The Insertion Reaction of 1CH2 into the Silicon-Carbon Bond
Frey, H. Monty,Walsh, Robin,Watts, Ivy M.
, p. 284 - 285 (2007/10/02)
Singlet methylene reacts with 1,1-dimethylsilacyclobutane to yield as well as the expected products formed by C-H insertion some 1,1-dimethylsilacyclopentane which strongly suggests that it can insert in the silicon-carbon bond.
Carbanion Rearrangements of ω-Phenyl-ω-(trimethylsilyl)alkyllithium Compounds: Intramolecular Reactions of Benzyltrimethylsilanes with a Carbon-Lithium Bond
Maercker, Adalbert,Stoetzel, Reinhard
, p. 1695 - 1706 (2007/10/02)
ω-Phenyl-ω-(trimethylsilyl)alkyllithium compounds show four out of five theoretically conceivable possibilities for intramolecular stabilization depending on the solvent and on the chain length n.While transmetalation of a methyl group at the silicon atom by a 1,(n+2) proton transfer is observed in any case, the intramolecular 1,n shift of the benzylic proton does only take place with n >/= 4.The main reaction, however for n = 3 and 4 only, is represented by the 1,n trimethylsilyl shift via a cyclic ate complex as an intermediate which partly splits off methyllithium yielding the corresponding silacycloalkane derivatives.In going from diethyl ether to THF as the solvent, the silyl shifts are more accelerated than the proton shifts.In no case, however, a Grovenstein-Zimmermann rearrangement involving phenyl migration took place.Degenerate silyl shifts starting from α-deuterated ω-(trimethylsilyl)alkyllithium compounds could not be detected either.Only by introduction of a second trimethylsilyl group into the 3 position a 1,3-(C -> C)-trimethylsilyl shift is initiated again.
