81411-68-9 Usage
Uses
Since the provided materials do not specify the applications of 3-Bromo-1H-pyrazolo[3,4-b]pyrazine, it is not possible to list its uses based on the given information. However, it is important to note that the compound's potential applications may be discovered through further research and development in various fields such as pharmaceuticals, materials science, or chemical engineering. It is recommended to consult scientific literature or conduct experiments to determine the specific uses and benefits of 3-Bromo-1H-pyrazolo[3,4-b]pyrazine in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 81411-68-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,4,1 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 81411-68:
(7*8)+(6*1)+(5*4)+(4*1)+(3*1)+(2*6)+(1*8)=109
109 % 10 = 9
So 81411-68-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H3BrN4/c6-4-3-5(10-9-4)8-2-1-7-3/h1-2H,(H,8,9,10)
81411-68-9Relevant academic research and scientific papers
Neighbouring Group Participation in Formation of Condensed Azines. Formation of Pyrazolo(3,4-b)pyrazines, Isoxazolo(4,5-b)pyrazines and Isothiazolo(5,4-b)pyridine (Heterocycles, CCX)
Kocevar, Marjan,Vercek, Bojan,Stanovnik, Branko,Tisler, Miha
, p. 731 - 744 (2007/10/02)
Pyrazine- and pyridinecarboxamidoximes with an amino, potentially tautomeric hydroxy or mercapto group in ortho position could be transformed in the appropriate condensed azines.In this manner, representatives of pyrazolo(3,4-b)pyrazine, isoxazolo(4,5-b)pyrazine and isothiazolo(5,4-b)pyridine ring system were synthesized and some transformations investigated. - Keywords: Cyclization with N-N, N-O or N-S bond formation; Heterocyclic compounds
NEW SYNTHETIC APPROACH FOR PYRAZOLOPYRAZINES AND ISOXAZOLOPYRAZINES
Kocevar, Marjan,Tisler, Miha,Stanovnik, Branko
, p. 339 - 342 (2007/10/02)
A new synthetic approach has been developed for the synthesis of pyrazolepyrazines (7) and isoxazolopyrazines (22) from the corresponding substituted pyrazines.
