27020-96-8 Usage
Uses
Used in Chemical Synthesis:
3-Trichloromethylbenzonitrile is used as a key intermediate in the production of various organic compounds, playing a crucial role in the synthesis process due to its reactive nature and ability to be transformed into a range of end products.
Used in Pesticide Production:
In the agricultural industry, 3-Trichloromethylbenzonitrile is utilized as an intermediate for the creation of pesticides. Its chemical properties make it a valuable component in developing effective pest control solutions.
Used in Pharmaceutical Manufacturing:
3-Trichloromethylbenzonitrile is employed as a precursor in the synthesis of pharmaceuticals. Its unique structure contributes to the development of new drugs, potentially enhancing treatment options for various medical conditions.
Used in Dye and Pigment Synthesis:
3-TRICHLOROMETHYLBENZONITRILE is also used as a precursor in the production of dyes and pigments for the textile, paint, and printing industries. Its ability to form a variety of colorants makes it an important substance in these sectors.
Used in Research and Development:
3-Trichloromethylbenzonitrile is utilized in research laboratories for the development of new chemical processes and the exploration of its potential applications in various fields, including material science and medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 27020-96-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,0,2 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 27020-96:
(7*2)+(6*7)+(5*0)+(4*2)+(3*0)+(2*9)+(1*6)=88
88 % 10 = 8
So 27020-96-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H4Cl3N/c9-8(10,11)7-3-1-2-6(4-7)5-12/h1-4H
27020-96-8Relevant academic research and scientific papers
Tele nucleophilic aromatic substitutions in 1-nitro-3- and 1,3-dinitro- 5-trichloromethylbenzene, and 3-trichloromethylbenzonitrile. A new synthesis of the 1,4-benzothiazine-3(4H)-one ring system from 3 nitrobenzoic acid
Giannopoulos, Thomas,Ferguson, John R.,Wakefield, Basil J.,Varvounis, George
, p. 447 - 453 (2007/10/03)
3-Trichloromethylnitrobenzene 2, 1,3-dinitro-5-trichloromethylbenzene 13 and 3-trichloromethylbenzonitrile 18 react with sodium methoxide to give 4- methoxy-3-nitrobenzaldehyde 6, 4-methoxy-3,5-dinitrobenzaldehyde 15 and 5- dimethoxymethyl-2-methoxybenzonitrile 19, respectively. Compounds 2 and 13 react with methyl thioglycolate to afford dichloromethylacetates 7 and 16, respectively. These products are the result of tele nucleophilic aromatic substitution. Compound 18 reacted with methyl thioglycolate to give acetate 20 resulting from nucleophilic displacement of cyanide. Reductive cyclisation of 7 afforded benzothiazine 11. (C) 2000 Elsevier Science Ltd.
