50998-17-9 Usage
Uses
Used in Pharmaceutical Synthesis:
6-Bromoquinoxaline is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and reactivity allow for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, 6-Bromoquinoxaline serves as a starting material for the production of various agrochemicals. Its properties enable the creation of effective compounds for pest control and crop protection.
Used in Dye and Pigment Manufacturing:
6-Bromoquinoxaline is utilized in the manufacturing of dyes and pigments due to its chemical properties. It contributes to the development of vibrant and stable colorants for various applications, including textiles, plastics, and inks.
Used in Heterocyclic Compound Preparation:
6-Bromoquinoxaline is employed as a starting material in the preparation of various heterocyclic compounds. Its unique structure allows for the synthesis of complex molecules with potential applications in various fields, such as medicine, materials science, and chemical research.
Check Digit Verification of cas no
The CAS Registry Mumber 50998-17-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,9,9 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 50998-17:
(7*5)+(6*0)+(5*9)+(4*9)+(3*8)+(2*1)+(1*7)=149
149 % 10 = 9
So 50998-17-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H5BrN2/c9-6-1-2-7-8(5-6)11-4-3-10-7/h1-5H
50998-17-9Relevant academic research and scientific papers
Bromination of quinoxaline and derivatives: Effective synthesis of some new brominated quinoxalines
U?ar, Sefa,E?siz, Sel?uk,Da?tan, Arif
, p. 1618 - 1632 (2017/03/08)
The synthesis of brominated quinoxaline derivatives starting from several kinds of quinoxaline by different bromination strategies was studied. First the synthesis of some brominated quinoxalines was accomplished along with the development of an alternative and effective synthesis of some known compounds. A new, clean, and effective synthetic method for selective reduction of quinoxaline to 1,2,3,4-tetrahydroquinoxaline was also developed. The products obtained were characterized by means of NMR spectroscopy, elemental analyses, and mass spectrometry.