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18301-86-5

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18301-86-5 Usage

General Description

3-Cyanopropyltrimethylsilane is a chemical compound with the molecular formula C7H15NSi. It is an organosilicon compound containing a cyano group, a propyl chain, and three trimethylsilyl groups. 3-CYANOPROPYLTRIMETHYLSILANE is commonly used as a reagent in organic synthesis, particularly in the production of various organosilicon compounds and polymers. It is also used as a surface modifier in the production of surface coatings and functionalized polymers. Additionally, 3-Cyanopropyltrimethylsilane is utilized as an intermediate in the manufacturing of pharmaceuticals and agrochemicals. Due to its versatile properties and applications, this chemical plays a significant role in the synthesis of various 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.

18301-86-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-trimethylsilylbutanenitrile

1.2 Other means of identification

Product number -
Other names 4-Trimethylsilyl-butyronitril

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:18301-86-5 SDS

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.

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