5315-73-1 Usage
Uses
Used in Pharmaceutical Industry:
IMIDAZO[1,2-A]PYRIDINE, 3-CHLOROis used as a building block for the synthesis of various pharmaceuticals due to its antiviral, antibacterial, and antitumor properties. It contributes to the development of new drugs that can potentially treat a wide range of diseases and conditions.
Used in Agrochemical Industry:
IMIDAZO[1,2-A]PYRIDINE, 3-CHLOROis used as a building block for the synthesis of various agrochemicals, leveraging its biological activities to create compounds that can protect crops from pests and diseases, thereby increasing agricultural productivity.
Used in Dye and Pigment Production:
IMIDAZO[1,2-A]PYRIDINE, 3-CHLOROis used as an intermediate in the production of dyes and pigments, contributing to the creation of a diverse range of colorants for various applications, including textiles, plastics, and printing inks.
Used in Organic Chemical Synthesis:
IMIDAZO[1,2-A]PYRIDINE, 3-CHLOROis used as an intermediate in the synthesis of other organic chemicals, showcasing its versatility and importance in the field of organic chemistry. Its unique structure allows for the development of new compounds with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 5315-73-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,1 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5315-73:
(6*5)+(5*3)+(4*1)+(3*5)+(2*7)+(1*3)=81
81 % 10 = 1
So 5315-73-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H18N2O2S/c1-18(2,3)15(21)11-23-17-20-19-16(22-17)14-9-8-12-6-4-5-7-13(12)10-14/h4-10H,11H2,1-3H3
5315-73-1Relevant academic research and scientific papers
Synergy of Anodic Oxidation and Cathodic Reduction Leads to Electrochemical C—H Halogenation
Zhou, Zhilin,Yuan, Yong,Cao, Yangmin,Qiao, Jin,Yao, Anjin,Zhao, Jing,Zuo, Wanqing,Chen, Wenjie,Lei, Aiwen
supporting information, p. 611 - 615 (2019/05/10)
We herein uncovered an electrochemical C—H halogenation protocol that synergistically combines anodic oxidation and cathodic reduction for C—X bond formation. The reaction was demonstrated under exogenous-oxidant-free conditions. Moreover, this is the first example of activating CBr4, CHBr3, and CCl3Br under electrochemical conditions.
Transition-metal-free regioselective C-H halogenation of imidazo[1,2-: A] pyridines: Sodium chlorite/bromite as the halogen source
Li, Junxuan,Tang, Jiayi,Wu, Yuanheng,He, Qiuxing,Yu, Yue
, p. 5058 - 5062 (2018/04/27)
A facile transition-metal-free regioselective halogenation of imidazo[1,2-a]pyridines using sodium chlorite/bromite as the halogen source is presented. The reaction has provided an efficient method for the formation of C-Cl or C-Br bonds to synthesize 3-c
