106864-97-5 Usage
Uses
Used in Pharmaceutical Industry:
(1-cyanoethyl)(dimethyl)silyl 2-(4-chloro-2-methylphenoxy)propanoate is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and silyl ester functionality contribute to the development of new drugs with improved properties and therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical industry, (1-cyanoethyl)(dimethyl)silyl 2-(4-chloro-2-methylphenoxy)propanoate is utilized as a crucial component in the production of agrochemicals. Its versatility and stability make it suitable for the synthesis of effective and environmentally friendly pesticides, herbicides, and other agricultural chemicals.
Used in Advanced Materials Development:
(1-cyanoethyl)(dimethyl)silyl 2-(4-chloro-2-methylphenoxy)propanoate is also employed in the development of advanced materials. Its unique structure and properties allow it to be incorporated into the synthesis of innovative materials with potential applications in various fields, such as electronics, coatings, and composites.
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.
