193358-40-6 Usage
Uses
Used in Coatings Industry:
P-BIS(TRIMETHOXYSILYLMETHYL)BENZENE is used as a bonding agent for enhancing the adhesion and durability of coatings on various surfaces, such as glass, metals, and ceramics. Its ability to form stable bonds with these substrates contributes to the improved performance and longevity of the coatings.
Used in Adhesives Industry:
In the adhesives industry, P-BIS(TRIMETHOXYSILYLMETHYL)BENZENE is used as a component in the formulation of adhesives that offer strong and long-lasting bonds between different materials. Its compatibility with both organic and inorganic materials makes it a valuable addition to adhesive formulations.
Used in Sealants Industry:
P-BIS(TRIMETHOXYSILYLMETHYL)BENZENE is used as a key ingredient in sealant formulations, providing excellent bonding properties and resistance to environmental factors. Its ability to form durable bonds with various substrates ensures the effectiveness and longevity of the sealants in applications such as construction and automotive industries.
Used in Composites Industry:
In the composites industry, P-BIS(TRIMETHOXYSILYLMETHYL)BENZENE is used as a reinforcing agent to improve the mechanical properties and durability of composite materials. Its ability to form strong bonds with both organic and inorganic components contributes to the overall strength and stability of the composites.
Used in Organic Synthesis:
P-BIS(TRIMETHOXYSILYLMETHYL)BENZENE is used as a reagent in organic synthesis processes, where its unique molecular structure allows for the creation of new compounds with desired properties. Its benzene rings and trimethoxysilyl groups provide a stable and reactive platform for various chemical reactions.
Used in Surface Modification Processes:
P-BIS(TRIMETHOXYSILYLMETHYL)BENZENE is used as a surface modifier to alter the properties of materials, such as improving their resistance to wear, enhancing their adhesion, or providing specific chemical functionalities. Its ability to form siloxane bonds with substrates through hydrolysis and condensation reactions makes it a suitable candidate for surface modification applications.
Check Digit Verification of cas no
The CAS Registry Mumber 193358-40-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,3,5 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 193358-40:
(8*1)+(7*9)+(6*3)+(5*3)+(4*5)+(3*8)+(2*4)+(1*0)=156
156 % 10 = 6
So 193358-40-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H26O6Si2/c1-15-21(16-2,17-3)11-13-7-9-14(10-8-13)12-22(18-4,19-5)20-6/h7-10H,11-12H2,1-6H3
193358-40-6Relevant academic research and scientific papers
Synthesis and characterization of bis(trialkoxysilymethyl) arenes from related bis(trichlorosilylmethyl)arenes. Comparisons between some organosilicate xerogel materials derived from both
Carr, Stuart W.
, p. 865 - 872 (2007/10/03)
A series of bis(trialkoxysilylmethyl)aryl compounds 1-17 {[(RO)3SiCH2]2Ar, R = Me, Et, Pr, Bu, Ar = 1,4-C6H4; R = Et, Pr, Bu, Ar = l,4-C6H2Me2-2,6; R = Et, Pr, Bu, Ar = l,4-C6Me4-2,3,5,6; R = Et, Pr, Bu, Ar = 1,3-C6H4; R = Bu, Ar = 1,2-C6H4; R = Et, Pr, Bu, Ar=9,10-C14H8} prepared from the related bis(trichlorosilylmethyl)aryl compounds and characterised by 1H, 13C and 29Si NMR and IR spectroscopy, and high resolution mass spectrometry. The X-ray crystal structures of two of the bis(trichlorosilylmethyl)aryl precursor compounds are reported. Organosilicate xerogels prepared from the precursors 2, 7 and 12 are discussed. These have been studied by a combination of solid state NMR spectroscopy, scanning electron microscopy (one case) and nitrogen sorption porosimetry and their properties compared with those of xerogels derived from related bis(trichlorosilylmethyl)arenes.
