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3-CYANOPROPYLTRIMETHOXYSILANE, with the molecular formula C6H13NO3Si, is a silane coupling agent characterized by a trimethoxysilyl functional group. It plays a pivotal role in the creation of adhesion promoters, surface modifiers, and crosslinking agents across a spectrum of industrial applications. This versatile chemical is instrumental in the synthesis of organosilicon compounds and in the modification of surfaces to bolster adhesion and compatibility with a variety of materials.

55453-24-2

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55453-24-2 Usage

Uses

Used in Chemical Synthesis:
3-CYANOPROPYLTRIMETHOXYSILANE is used as a silane coupling agent for the synthesis of organosilicon compounds, enhancing the reactivity and properties of these materials for diverse applications.
Used in Surface Modification:
3-CYANOPROPYLTRIMETHOXYSILANE is used as a surface modifier to improve the adhesion and compatibility of materials, facilitating their integration with other substances in various industrial processes.
Used in Manufacturing of Coatings, Adhesives, and Sealants:
3-CYANOPROPYLTRIMETHOXYSILANE is used as a crosslinking agent in the formulation of these products, enhancing their durability, flexibility, and performance in a range of applications.
Used in Electronics Industry:
3-CYANOPROPYLTRIMETHOXYSILANE is used as a component in the production of silicone rubbers and resins, contributing to the development of materials with specific electrical and thermal properties for use in electronic devices and components.
Used in Automotive Industry:
3-CYANOPROPYLTRIMETHOXYSILANE is used in the formulation of materials for automotive applications, such as sealants and coatings, to ensure high performance and resistance to environmental factors.
Used in Construction Industry:
3-CYANOPROPYLTRIMETHOXYSILANE is used in the production of construction materials, including sealants and adhesives, to improve their bonding strength and durability in building applications.
Used in Pharmaceutical Production:
3-CYANOPROPYLTRIMETHOXYSILANE is used in the manufacturing of specialty chemicals and pharmaceuticals, potentially contributing to the development of new drugs and medicinal products.

Check Digit Verification of cas no

The CAS Registry Mumber 55453-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,4,5 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55453-24:
(7*5)+(6*5)+(5*4)+(4*5)+(3*3)+(2*2)+(1*4)=122
122 % 10 = 2
So 55453-24-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H15NO3Si/c1-9-12(10-2,11-3)7-5-4-6-8/h4-5,7H2,1-3H3

55453-24-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-trimethoxysilylbutanenitrile

1.2 Other means of identification

Product number -
Other names EINECS 259-646-9

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:55453-24-2 SDS

55453-24-2Downstream Products

55453-24-2Relevant academic research and scientific papers

A novel tin-free procedure for alkyl radical reactions

Benati, Luisa,Leardini, Rino,Minozzi, Matteo,Nanni, Daniele,Scialpi, Rosanna,Spagnolo, Piero,Strazzari, Samantha,Zanardi, Giuseppe

, p. 3598 - 3601 (2007/10/03)

Desulfuration as a source of alkyl radicals: The addition of alkylsulfanyl radicals to isocyanides gives the corresponding alkyl radicals. This methodology can replace the usual tin-mediated radical procedures and allows for the generation of tertiary, secondary, and even nonstabilized primary radicals that can be used efficiently in reductive defunctionalizations and intermolecular additions to electron-rich olefins (see scheme).

Method and apparatus for the preparation of cyanoalkyl-alkoxysilanes

-

, (2008/06/13)

In a method of preparing cyanoalkyl-akoxysilanes, which is suitable for the production of these silanes on a large technical scale, the reaction of a chloroalkyl-alkoxysilane with an alkali metal cyanide in the presence of a solvent takes place in a stirring reactor which is provided with means for loading these starting materials and with an outlet opening for the alkali metal chloride by-product, and which is connected through a bypass valve to a column with a superimposed condenser. After the reaction in the reactor has ended, first the solvent is distilled out through the column and then the main part of the cyanosilane, and then the rest of the cyanosilane is distilled out while bypassing the column. The alkali metal chloride is then removed from the reactor through a lock.

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