30720-84-4 Usage
Uses
Used in Energetic Materials Industry:
4-AMINO-FURAZAN-3-CARBOXYLIC ACID METHYLAMIDE is used as an energetic material for its high reactivity and explosive properties, making it a potential candidate for applications in explosives and propellants. Its sensitivity to heat and mechanical shock, however, requires extreme caution in handling and storage to ensure safety.
Due to the hazardous nature of 4-AMINO-FURAZAN-3-CARBOXYLIC ACID METHYLAMIDE, its applications are primarily limited to specialized industries that require high-energy materials. Further research and development may explore safer methods of utilization or stabilization to expand its potential uses while mitigating risks.
Check Digit Verification of cas no
The CAS Registry Mumber 30720-84-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,7,2 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 30720-84:
(7*3)+(6*0)+(5*7)+(4*2)+(3*0)+(2*8)+(1*4)=84
84 % 10 = 4
So 30720-84-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H6N4O2/c1-6-4(9)2-3(5)8-10-7-2/h1H3,(H2,5,8)(H,6,9)
30720-84-4Relevant academic research and scientific papers
IMIDAZO[1,2-B]PYRIDAZINE IL-17A INHIBITORS
-
Page/Page column 23; 64, (2020/07/25)
The invention provides certain difluorocyclohexyl-imidazopyridazinyl-imidazolidinone compounds of formula II as IL-17A inhibitors, pharmaceutical compositions thereof, and methods of using a compound of formula II to treat certain symptoms of psoriasis, rheumatoid arthritis or multiple sclerosis.
A new preparative method and some chemical properties of 4-R-furazan-3-carboxylic acid amidrazones
Stepanov, Andrei I.,Sannikov, Vladimir S.,Dashko, Dmitry V.,Roslyakov, Alexey G.,Astrat'Ev, Alexander A.,Stepanova, Elena V.
, p. 350 - 360 (2016/01/12)
[Figure not available: see fulltext.] An alternative method has been developed for the preparation of 4-R-furazan-3-carboxylic acid amidrazones (R = OMe, NH2, substituted amino group) by reductive opening of 1,2,4-oxadiazole ring in 4-R derivatives of (1,2,4-oxadiazol-3-yl)furazans by the action of hydrazine. The starting 1,2,4-oxadiazoles were synthesized from 4-aminofurazan-3-carboxylic acid amidoxime. Some chemical properties of the obtained compounds were studied.
