50874-31-2 Usage
Uses
Used in Military Applications:
(-)-ALPHA-(2,4,5,7-TETRANITRO-9-FLUORENYLIDENEAMINOXY)PROPIONIC ACID is used as an explosive agent for its high energy output and sensitivity, suitable for various military operations and requirements.
Used in Industrial Applications:
In the industrial sector, (-)-ALPHA-(2,4,5,7-TETRANITRO-9-FLUORENYLIDENEAMINOXY)PROPIONIC ACID is utilized as an oxidizer in propellants and explosives due to its high nitrogen content, enhancing the performance of these materials.
Used in Research and Development of Energetic Materials:
(-)-ALPHA-(2,4,5,7-TETRANITRO-9-FLUORENYLIDENEAMINOXY)PROPIONIC ACID is employed as a potential candidate in the development of new energetic materials and formulations, owing to its unique molecular structure and energetic properties.
Safety Precautions:
Due to the high sensitivity and potential hazards associated with (-)-ALPHA-(2,4,5,7-TETRANITRO-9-FLUORENYLIDENEAMINOXY)PROPIONIC ACID, it is crucial to implement proper handling and safety measures when working with (-)-ALPHA-(2,4,5,7-TETRANITRO-9-FLUORENYLIDENEAMINOXY)PROPIONIC ACID to mitigate risks and ensure safety.
Check Digit Verification of cas no
The CAS Registry Mumber 50874-31-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,8,7 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 50874-31:
(7*5)+(6*0)+(5*8)+(4*7)+(3*4)+(2*3)+(1*1)=122
122 % 10 = 2
So 50874-31-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H9N5O11/c1-6(16(22)23)32-17-15-9-2-7(18(24)25)4-11(20(28)29)13(9)14-10(15)3-8(19(26)27)5-12(14)21(30)31/h2-6H,1H3,(H,22,23)/t6-/m1/s1
50874-31-2Relevant academic research and scientific papers
Application of NMR Spectroscopy of Chiral Association Complexes. 13.Electron Donor-acceptor Complexes between Racemic Carbazolocarbazoles and an Optically Active Acceptor
Icli, Siddik,Burgemeister, Thomas,Mannschreck, Albrecht,Zander, Maximilian
, p. 145 - 150 (2007/10/02)
Strong electron donor-acceptor (EDA) asociation between carbazolocarbazoles and an optically active tetranitrofluorenone derivative was detected by UV-visible spectroscopy and by 1H NMR shifts. 1H NMR splitting at low temperatures are due ti diastereomeric association complexes and, thus, prove the chirality of carbazolocarbazoles.
