193358-40-6 Usage
General Description
P-Bis(trimethoxysilylmethyl)benzene is a chemical compound that possesses a unique combination of organic and inorganic properties. It is widely used in industries due to its ability to form stable and durable bonds with a plethora of substrates, including glass, metals, ceramics, and polymers. Notably, it acts as a linker molecule that can bridge organic and inorganic materials, which makes it suitable for diverse applications like coatings, adhesives, sealants, and composites. It is also utilized in organic synthesis and surface modification processes. Its unique molecular structure lends itself well to these tasks, as it contains benzene rings, which are extremely stable and resistant to reactions, and trimethoxysilyl groups, which can undergo hydrolysis and condensation reactions to form siloxane bonds with substrates.
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 articles and documents
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.
