89980-70-1 Usage
Uses
Used in Pharmaceutical Synthesis:
QUINOXALINE, 6-BROMO-1,2,3,4-TETRAHYDROis used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic benefits.
Used in Agrochemical Synthesis:
QUINOXALINE, 6-BROMO-1,2,3,4-TETRAHYDROis also utilized as a building block in the creation of agrochemicals, playing a role in the development of pesticides and other agricultural products to improve crop protection and yield.
Used in Organic Synthesis:
QUINOXALINE, 6-BROMO-1,2,3,4-TETRAHYDROis employed as a versatile component in organic synthesis, enabling the formation of a wide range of organic compounds for various applications.
Used in Material Science:
In the field of material science, QUINOXALINE, 6-BROMO-1,2,3,4-TETRAHYDRO- has potential applications in the development of new materials with specific properties, such as those used in electronics, sensors, or other advanced technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 89980-70-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,9,8 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 89980-70:
(7*8)+(6*9)+(5*9)+(4*8)+(3*0)+(2*7)+(1*0)=201
201 % 10 = 1
So 89980-70-1 is a valid CAS Registry Number.
89980-70-1Relevant 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.
