3121-75-3 Usage
Uses
Used in the Rubber Industry:
CHLOROMETHYLDIMETHYL-N-BUTYLSILANE is used as a coupling agent and adhesion promoter to enhance the bonding properties between rubber and other materials, improving the overall performance and durability of rubber products.
Used in the Plastics Industry:
In the plastics sector, CHLOROMETHYLDIMETHYL-N-BUTYLSILANE functions as a coupling agent to improve the compatibility and interfacial adhesion between different plastic components, leading to enhanced mechanical properties and performance of the final plastic products.
Used in the Coatings Industry:
CHLOROMETHYLDIMETHYL-N-BUTYLSILANE is utilized as a coupling agent in the production of coatings to promote adhesion between the coating and the substrate, resulting in improved durability, resistance, and overall performance of the coatings.
Used in Surface Modification:
CHLOROMETHYLDIMETHYL-N-BUTYLSILANE is used as a surface modifier across various industries to enhance the bonding properties of materials, leading to improved material performance and durability.
Used in the Synthesis of Organosilicon Compounds:
As a key intermediate, CHLOROMETHYLDIMETHYL-N-BUTYLSILANE is employed in the synthesis of other organosilicon compounds, contributing to the development of new materials and products in the field of silicone chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 3121-75-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,2 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3121-75:
(6*3)+(5*1)+(4*2)+(3*1)+(2*7)+(1*5)=53
53 % 10 = 3
So 3121-75-3 is a valid CAS Registry Number.
3121-75-3Relevant academic research and scientific papers
Process for the preparation of lactic acid silyl esters
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, (2008/06/13)
Novel lactic acid silyl esters of the formula STR1 in which R represents alkyl or aryl, are obtained by a new process which comprises reacting a lactic acid of the formula STR2 with a chloromethylsilane of the formula STR3 in which R has the meaning indicated above, in the presence of a tertiary amine and, if appropriate, in the presence of an additional diluent, at temperatures between 50° and 120° C.
SYNTHESE UND UMLAGERUNGSREAKTIONEN VON o-FUNKTIONELLEN PHENYLLITHIUM- UND PHENYLNATRIUM DERIVATEN DER IVB UND VB-ELEMENTE
Heinicke, J.,Nietzschmann, E.,Tzschach, A.
, p. 1 - 8 (2007/10/02)
While o-substituted bromobenzene derivatives of the type o-BrC6H4XERn (X = O, S; ERn = SiMe3) and n-BuLi undergo metal halogen exchange followed by silyl-X -> C rearrangement, the corresponding compounds of phosphorus, arsenic or tin are split at the E-X bond. o-Metal derivatives o-MI-C6H4XERn (X = O, NMe; E = P, As, Sn) of these elements may be generated, however, by direct reaction with sodium or lithium.They are unstable and furnish o-hydroxy- and o-aminophenyl element(IV, V) derivatives via an intramolecular anionic rearrangement.
