50407-18-6 Usage
Uses
Used in Organic Synthesis:
2,3-dimethyl-2H-indazole is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the development of new compounds and materials.
Used in Pharmaceutical Research:
In pharmaceutical research, 2,3-dimethyl-2H-indazole serves as a valuable tool for the investigation of drug candidates and the study of biological processes, aiding in the advancement of medical treatments.
Used in Pharmaceutical Production:
2,3-dimethyl-2H-indazole is employed in the production of pharmaceutical products, where it may act as an intermediate or a key component in the synthesis of active pharmaceutical ingredients.
Used in Agrochemicals:
2,3-dimethyl-2H-indazole is also utilized in the creation of agrochemicals, playing a role in the development of pesticides, herbicides, and other agricultural products to enhance crop protection and yield.
Used in Materials Science:
2,3-dimethyl-2H-indazole has potential applications in materials science, where it may contribute to the design and synthesis of novel materials with specific properties for various industrial applications.
Used as a Flavoring Agent in the Food Industry:
In the food industry, 2,3-dimethyl-2H-indazole is used as a flavoring agent to impart unique taste profiles to food products, enhancing the sensory experience for consumers.
Check Digit Verification of cas no
The CAS Registry Mumber 50407-18-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,4,0 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 50407-18:
(7*5)+(6*0)+(5*4)+(4*0)+(3*7)+(2*1)+(1*8)=86
86 % 10 = 6
So 50407-18-6 is a valid CAS Registry Number.
50407-18-6Relevant articles and documents
Direct N-Alkylation and Kemp Elimination Reactions of 1-Sulfonyl-1H-Indazoles
Tang, Meng,Chu, Bingjie,Chang, Xiaowei
, p. 2109 - 2116 (2018/07/31)
The reactions of 1-sulfonyl-1H-indazoles under basic conditions are discussed, and the direct N-alkylation and Kemp elimination reactions of these compounds are reported. A series of 2-(p-tosylamino)benzonitriles and N-alkyl indazoles were prepared in good yields. Moreover, the 2-(p-tosylamino)benzonitriles could be transformed into a diverse range of important derivatives in a one-pot reaction. This method was successfully applied to the total syntheses of quindolinone and cryptolepinone; quindolinone was prepared in a one-pot reaction from 1-sulfonyl-1H-indazole.
Convenient method for the 3-functionalization of isoindazoles
Bunnell, Aaron,O'Yang, Counde,Petrica, Andra,Soth, Michael J.
, p. 285 - 293 (2007/10/03)
The C-3 position of isoindazoles is readily functionalized by metalation with lithium diisopropylamide followed by reaction with a variety of electrophiles. Copyright Taylor & Francis LLC.
BENZOLOGOUS REISSERT COMPOUND FORMATION FROM 2-METHYLINDAZOLE
Uff, Barrie C.,Ho, Yee-Ping,Popp, Frank D.
, p. 1239 - 1246 (2007/10/02)
2-Methylindazole undergoes 1,4-addition on treatment under Reissert conditions.Methylation of the product in strong base leads to 2,3-dimethylindazole.
