73713-69-6 Usage
Uses
Used in Pharmaceutical Industry:
2,5-Dimethyl-4-nitrobenzonitrile is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be incorporated into the development of new drugs, contributing to the advancement of medicine.
Used in Agrochemical Industry:
In the agrochemical industry, 2,5-Dimethyl-4-nitrobenzonitrile serves as an essential component in the production of various agrochemicals. Its reactivity and chemical properties make it suitable for the development of effective pesticides and other agricultural chemicals.
Used in Dye and Pigment Production:
2,5-Dimethyl-4-nitrobenzonitrile is also used as an intermediate in the production of dyes and pigments. Its chemical properties enable the creation of a wide range of colors and shades, contributing to the diversity of colorants available in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 73713-69-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,7,1 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73713-69:
(7*7)+(6*3)+(5*7)+(4*1)+(3*3)+(2*6)+(1*9)=136
136 % 10 = 6
So 73713-69-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2O2/c1-6-4-9(11(12)13)7(2)3-8(6)5-10/h3-4H,1-2H3
73713-69-6Relevant academic research and scientific papers
Nitration of moderately deactivated arenes with nitrogen dioxide and molecular oxygen under neutral conditions. Zeolite-induced enhancement of regioselectivity and reversal of isomer ratios
Peng, Xinhua,Fukui, Naoyuki,Mizuta, Masayuki,Suzuki, Hitomi
, p. 2326 - 2335 (2007/10/03)
In the presence of zeolites, moderately deactivated arenes such as 1-nitronaphthalene, naphthonitriles, and methylated benzonitriles can be smoothly nitrated at room temperature by the combined action of nitrogen dioxide and molecular oxygen. The regioselectivity is considerably improved as compared with the conventional nitration methodology based on nitric and sulfuric acids. In some cases, the minor isomer became favoured to a significant extent, resulting in the reversal of ordinary isomer ratios of nitration products.
