155629-96-2 Usage
Uses
Given the provided materials, specific uses for Pyrido[2,3-b]pyrazine, 6-methyl(9CI) are not detailed. However, based on its classification and structure, it can be inferred that Pyrido[2,3-b]pyrazine, 6-methyl- (9CI) may have potential applications in various fields such as pharmaceuticals, materials science, or as an intermediate in the synthesis of other organic compounds. The exact uses would depend on the compound's properties, which are not specified in the provided materials. If further information becomes available, specific applications could be listed as follows:
Used in Pharmaceutical Industry:
Pyrido[2,3-b]pyrazine, 6-methyl(9CI) could be utilized as a pharmaceutical agent for [specific medical condition or purpose] due to its [particular biological activity or property].
Used in Materials Science:
In the field of materials science, Pyrido[2,3-b]pyrazine, 6-methyl(9CI) might serve as a component in the development of new materials with [desired properties], attributed to its [chemical or physical characteristics].
Used as a Synthesis Intermediate:
Pyrido[2,3-b]pyrazine, 6-methyl(9CI) could be employed as an intermediate in the synthesis of more complex organic compounds, potentially leading to the creation of novel molecules with [specific applications or uses].
Check Digit Verification of cas no
The CAS Registry Mumber 155629-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,6,2 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 155629-96:
(8*1)+(7*5)+(6*5)+(5*6)+(4*2)+(3*9)+(2*9)+(1*6)=162
162 % 10 = 2
So 155629-96-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H7N3/c1-6-2-3-7-8(11-6)10-5-4-9-7/h2-5H,1H3
155629-96-2Relevant academic research and scientific papers
Heterocyclizations in the pyrido[2,3-b]pyrazine series
Blache,Gueiffier,Chavignon,Teulade,Milhavet,Viols,Chapat,Dauphin
, p. 161 - 166 (2007/10/02)
In this paper, we report the results of heterocyclizations in the pyrido[2,3-b]pyrazine series to give the pyrido[2,3-e] or [3,2-e]pyrrolo[1,2- a]pyrazine. The Clauson-Kaas reaction on 2,3-diaminopyridine is investigated; regioselectivity on the 3-amino group is shown by 1H- and 13C-nmr. Synthesis and reactivity of the original pyrazino[2,3-g]indolizine series is also reported.
