5580-34-7 Usage
Uses
Used in Pharmaceutical Industry:
2,3-Dimethylbenzamide is used as a key building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its chemical structure allows for versatile modifications, making it a valuable component in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 2,3-Dimethylbenzamide serves as a fundamental component in the creation of pesticides and other agricultural chemicals, enhancing crop protection and yield.
Used in Dye and Pigment Production:
2,3-Dimethylbenzamide is utilized as an intermediate in the production of dyes and pigments, playing a crucial role in the coloration of various materials and products.
Used in Organic Compound Synthesis:
Beyond its applications in specific industries, 2,3-Dimethylbenzamide is a versatile intermediate for the synthesis of a wide range of organic compounds, broadening its utility in chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 5580-34-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,8 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5580-34:
(6*5)+(5*5)+(4*8)+(3*0)+(2*3)+(1*4)=97
97 % 10 = 7
So 5580-34-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO/c1-6-4-3-5-8(7(6)2)9(10)11/h3-5H,1-2H3,(H2,10,11)
5580-34-7Relevant academic research and scientific papers
Benzamide synthesis by direct electrophilic aromatic substitution with cyanoguanidine
Naredla, Rajasekhar Reddy,Klumpp, Douglas A.
experimental part, p. 4779 - 4781 (2012/09/07)
Cyanoguanidine is an inexpensive commodity chemical and it is found to be a useful reagent for the direct Friedel-Crafts carboxamidation of arenes. The reaction works best in an excess of Bronsted superacid, an observation suggesting the involvement of a superelectrophilic intermediate. Theoretical calculations indicate that the most stable diprotonated species involves protonation at the guanidine and cyano nitrogen atoms.
