18301-86-5 Usage
Description
3-CYANOPROPYLTRIMETHYLSILANE, with the molecular formula C7H15NSi, is an organosilicon compound that features a cyano group, a propyl chain, and three trimethylsilyl groups. It is known for its versatile properties and is widely utilized in various chemical processes and material syntheses.
Uses
Used in Organic Synthesis:
3-CYANOPROPYLTRIMETHYLSILANE is used as a reagent for the production of various organosilicon compounds and polymers, contributing to the synthesis of a broad range of materials with unique properties.
Used in Surface Modification:
In the industry of surface coatings and functionalized polymers, 3-CYANOPROPYLTRIMETHYLSILANE is used as a surface modifier, enhancing the performance characteristics of these materials.
Used in Pharmaceutical Manufacturing:
3-CYANOPROPYLTRIMETHYLSILANE is utilized as an intermediate in the manufacturing process of pharmaceuticals, playing a crucial role in the development of new drugs.
Used in Agrochemical Production:
3-CYANOPROPYLTRIMETHYLSILANE is also employed in the production of agrochemicals, where it serves as an intermediate, aiding in the synthesis of various agricultural chemicals that are essential for crop protection and enhancement.
Overall, 3-CYANOPROPYLTRIMETHYLSILANE's applications span across multiple industries, highlighting its importance in the synthesis of industrial and research-grade materials.
Check Digit Verification of cas no
The CAS Registry Mumber 18301-86-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,0 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18301-86:
(7*1)+(6*8)+(5*3)+(4*0)+(3*1)+(2*8)+(1*6)=95
95 % 10 = 5
So 18301-86-5 is a valid CAS Registry Number.
18301-86-5Relevant articles and documents
Infrared Spectrometric Studies of Cyanoalkyl Ligands Immobilized on Chromatographic Surfaces
Suffolk, B. R.,Gilpin, R. K.
, p. 596 - 601 (1985)
Long and intermediate chains of cyanoalkyl ligands were attached to porous silica-based material by using monoreactive chemistry, and short cyanoalkyl chains were attached by using mono-, di-, and trireactive chemistry.Subsequently, the microchemical structures of these materials were studied with Fourier transform infrared (FT-IR) techniques.In a nonpolar liquid (i.e., hexane) infrared spectra for the nitrile band were extremely broad and assymetrical.Deconvolution of these bands produced a doublet which suggested the presence of at least two different types of attached ligands.These bands support the idea of a certain population of nitrile groups which hydrogen bond with free surface silanol groups and a population of nitrile groups which sterically cannot hydrogen bond.This is possible by assuming a nonuniform distribution of groups.Groups bonded within a rich area or cluster would be restricted from surface interaction by surrounding groups or neighboring groups, whereas groups at the edges of such a cluster or groups bonded in sparcely populated areas could hydrogen bond.In a polar solvent (e.g., 1-butanol) the groups were displaced from the surface and showed ligand-solvent interaction.
