106864-97-5 Usage
General Description
The chemical compound "(1-cyanoethyl)(dimethyl)silyl 2-(4-chloro-2-methylphenoxy)propanoate" is a complex organic compound used in the synthesis of various pharmaceuticals, agrochemicals, and materials. It is a silyl ester that contains a cyanoethyl group, two dimethylsilyl groups, and a 2-(4-chloro-2-methylphenoxy)propanoate group. The silyl ester functionality provides stability and protection to the compound, allowing it to be used as a versatile intermediate in organic synthesis. (1-cyanoethyl)(dimethyl)silyl 2-(4-chloro-2-methylphenoxy)propanoate has potential applications in the production of pharmaceuticals and agrochemicals, as well as in the development of advanced materials. Overall, "(1-cyanoethyl)(dimethyl)silyl 2-(4-chloro-2-methylphenoxy)propanoate" is a key building block in the synthesis of various organic compounds with diverse industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 106864-97-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,8,6 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 106864-97:
(8*1)+(7*0)+(6*6)+(5*8)+(4*6)+(3*4)+(2*9)+(1*7)=145
145 % 10 = 5
So 106864-97-5 is a valid CAS Registry Number.
106864-97-5Relevant articles and documents
Gas Chromatographic and Mass Spectrometric Determination of Chlorophenoxy Acids and Related Herbicides as Their (Cyanoethyl)dimethylsilyl Derivatives
Bertrand, Michel J.,Ahmed, A. W.,Sarrasin, Benoit,Mallet, Victorin N.
, p. 1302 - 1306 (2007/10/02)
A method using (2-cyanoethyl)dimethyl(diethylamino)silane to form derivatives with phenoxy acid herbicides and related compounds is presented.Results obtained with 18 compounds demonstrate that the reaction is quantitative and complete within minutes at room temperature.The derivatives formed can readily be analyzed by gas chromatography using a selective nitrogen-phosphorus detector which eliminates the need for rigorous cleanup of the sample required for detection by electron capture.Response-concentration plots show that detection is linear over several decades with limits of detection being in the low picogram range for all compounds studied.Mass spectral analysis of the derivatives of the 18 compounds studied indicates that the spectra are highly specific showing characteristic ions at (M-54), (M-82), or (M-98) which are useful for structure confirmation or analysis at low levels by using selected ion monitoring.The analytical advantages of the approach for the analysis of acid herbicides are discussed.
