18407-13-1 Usage
Description
Di-n-hexyldiethoxysilan is a chemical compound with the formula C20H42O2Si. It is a silane coupling agent characterized by its ability to form strong chemical bonds with both organic and inorganic surfaces due to its structure, which includes two ethoxy groups and two hexyl groups attached to a silicon atom.
Uses
Used in Polymer Production:
Di-n-hexyldiethoxysilan is used as a coupling agent for enhancing the compatibility and adhesion between organic and inorganic materials in the production of polymers.
Used in Coatings Industry:
Di-n-hexyldiethoxysilan is used as a surface modifier to improve the adhesion and durability of coatings, making them more resistant to wear and environmental factors.
Used in Adhesives Manufacturing:
Di-n-hexyldiethoxysilan is used as a component in adhesive formulations to increase the bonding strength between different materials, particularly those involving both organic and inorganic components.
Used in Rubber and Plastics Industry:
Di-n-hexyldiethoxysilan is used to enhance the properties of rubber and plastics, contributing to their overall strength, durability, and resistance to water and other elements.
Used in Industrial Material Manufacturing:
Di-n-hexyldiethoxysilan is utilized in the manufacturing of various industrial materials to improve their overall performance, including their resistance to water and their structural integrity.
Check Digit Verification of cas no
The CAS Registry Mumber 18407-13-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,0 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18407-13:
(7*1)+(6*8)+(5*4)+(4*0)+(3*7)+(2*1)+(1*3)=101
101 % 10 = 1
So 18407-13-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H36O2Si/c1-5-9-11-13-15-19(17-7-3,18-8-4)16-14-12-10-6-2/h5-16H2,1-4H3
18407-13-1Relevant articles and documents
Convenient synthesis of alkoxyhalosilanes from hydrosilanes
Ohshita, Joji,Taketsugu, Ryosuke,Nakahara, Yuki,Kunai, Atsutaka
, p. 3258 - 3264 (2007/10/03)
Selective dehydrogenative coupling of di- and trihydrosilanes with alcohols catalyzed by PdCl2 or NiCl2 afforded alkoxyhydro- and dialkoxyhydrosilanes in good yield. Further treatment of the resulting alkoxyhydrosilanes with carbon tetrachloride or allyl bromide in the presence of the same catalyst led to the formation of alkoxychloro- and alkoxybromosilanes, respectively. Similar reactions of dialkoxyhydrosilanes with carbon tetrachloride afforded dialkoxychlorosilanes in good yield, although contamination of small amounts of trialkoxysilanes and alkoxydichlorosilanes was detected in the products. Selective substitution of the alkoxyhalosilanes with nucleophiles is also reported.
