143309-87-9 Usage
Uses
Used in Pharmaceutical Industry:
6,7-Dichloro-2-methyl-3-(trifluoromethyl)quinoxaline is used as a key intermediate in the synthesis of new drugs for its potent antimicrobial and antiparasitic properties. Its unique structure and versatile reactivity make it a promising candidate for the development of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 6,7-Dichloro-2-methyl-3-(trifluoromethyl)quinoxaline is utilized as a building block for the creation of new pesticides. Its antimicrobial and antiparasitic properties contribute to the development of effective solutions for pest control and crop protection.
Used in Synthesis of Bioactive Compounds:
6,7-Dichloro-2-methyl-3-(trifluoromethyl)quinoxaline is used as a valuable building block for the synthesis of various bioactive compounds due to its unique structure and versatile reactivity. This allows for the development of a wide range of applications in both the pharmaceutical and agrochemical sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 143309-87-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,3,0 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 143309-87:
(8*1)+(7*4)+(6*3)+(5*3)+(4*0)+(3*9)+(2*8)+(1*7)=119
119 % 10 = 9
So 143309-87-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H5Cl2F3N2/c1-4-9(10(13,14)15)17-8-3-6(12)5(11)2-7(8)16-4/h2-3H,1H3
143309-87-9Relevant academic research and scientific papers
19F NMR Studies on the Mechanism of Riboflavin Synthase. Synthesis of 6-(Trifluoromethyl)-7-oxo-8-(D-ribityl)lumazine and 6-(trifluoromethyl)-7-methyl-8-(D-ribityl)lumazine
Cushman, Mark,Patel, Hemantkumar H.,Scheuring, Johannes,Bacher, Adelbert
, p. 5630 - 5643 (2007/10/02)
The reactions of hexafluoropropene oxide (19), methyl trifluoropyruvate (21), and 1,1,1-trifluorobutane-2,3-dione (45) with a series of ortho diamines were investigated as an approach to the synthesis of trifluoromethyl-substituted quinoxalinones and luma
