5926-26-1 Usage
Description
Chloromethyltrimethoxysilane (CMTMS) is a trialkoxysilane with a chloromethyl organofunctional group, which contributes to its hydrophobic characteristics. This electron-withdrawing group enhances the mechanical properties of the molecule, making CMTMS a versatile silane-based precursor material for various applications.
Uses
Used in Chemical Synthesis:
Chloromethyltrimethoxysilane is used as a chemical intermediate for the synthesis of 1-methyl-1H-benzimidazole (MBI)-modified nanoparticles. This application takes advantage of CMTMS's reactivity and ability to form stable bonds with other molecules, leading to the creation of nanoparticles with specific properties.
Used in Material Science:
In the field of material science, Chloromethyltrimethoxysilane is used as a precursor for the preparation of mesoporous monolithic silica gels. These gels have unique properties, such as high surface area and tunable pore size, which make them suitable for various applications, including catalysis, drug delivery, and gas separation.
Used in Surface Coating Industry:
Chloromethyltrimethoxysilane is used as a silane-based precursor material for the preparation of surface enhancement coatings. The hydrophobic nature and improved mechanical properties of CMTMS contribute to the development of coatings with enhanced durability, adhesion, and resistance to environmental factors.
Used in Silane-Based Products:
CMTMS is also utilized in the production of other silane-based products, leveraging its unique properties to create materials with specific characteristics for various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 5926-26-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,2 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5926-26:
(6*5)+(5*9)+(4*2)+(3*6)+(2*2)+(1*6)=111
111 % 10 = 1
So 5926-26-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H11ClO3Si/c1-6-9(4-5,7-2)8-3/h4H2,1-3H3
5926-26-1Relevant articles and documents
(Iodomethyl)fluorosilanes: Synthesis and Reactions
Gostevskii,Lazareva
, p. 2084 - 2088 (2018/12/11)
The methods of synthesis of bifunctional (iodomethyl)fluorosilanes of general formula ICH2SiMenF3–n (n = 0, 2) have been elaborated; the structure was proved by 1H, 13C, 29Si NMR spectroscopy. The reaction of (iodomethyl)dimethylfluorosilane with O-trimethylsilyl derivative of N,N'-dimethylhydrazide of trifluoroacetic acid gives rise to the formation of 2,2,4,4-tetramethyl-6-(trifluoromethyl)-3,4-dihydro-2Н-1,4,5,2-oxadiasilin-4-ium iodide with tetracoordinate silicone atom.
Dendrimers with 1, 3, 5-Trisilacyclohexane as Core Unit
Weisheim, Eugen,Neumann, Beate,Stammler, Hans-Georg,Mitzel, Norbert W.
supporting information, p. 329 - 334 (2016/02/27)
1, 1, 3, 3, 5, 5-Hexavinyl-1, 3, 5-trisilacylohexane [Si(CH=CH2)2CH2]3 was synthesized and hydrosilylated with trichlorosilane to afford the first generation of a dendrimer. Conversion of this molecule with 18 Si-Cl functions on its surface with an excess of vinylmagnesium bromide yielded the 18-fold vinylated dendrimer. The new compounds were identified by elemental analyses, multi-nuclear NMR spectroscopy, and mass spectrometry. Crystal structures were obtained for [Si(CH=CH2)2CH2]3 and [Si(CH2-CH2SiCl3)2CH2]3.
METHOD FOR PRODUCING ALKOXY HYDROSILANE
-
Paragraph 0032, (2013/05/09)
The present invention provides a method for producing an alkoxyhydrosilane. Provided is a method for producing an alkoxyhydrosilane (A), comprising a reaction of a halohydrosilane (B) represented by formula (1) : H-SiR2c(CR13-bYb)aX3-a-c wherein R1 is a hydrogen atom or a hydrocarbon group; R2 is a hydrocarbon group; X is a halogen atom; Y is a hetero substituent; a is 1 or 2; b is 1, 2 or 3; and c is 1 or 0, with an orthoester (C) at a molar ratio of the orthoester (C) to the halohydrosilane (B) of constantly not less than 1, to produce the alkoxyhydrosilane (A) represented by formula (3) : H-SiR2c(CR13-bYb)a(OR8)3-a-c wherein R8 is a hydrocarbon group.
