68159-09-1 Usage
Chemical structure
Contains a chlorine and nitro group, as well as an indazole ring.
Classification
An ethanone, indicating the presence of a ketone functional group.
Applications
Likely has applications in organic synthesis and medicinal chemistry due to its unique structure and potentially reactive functional groups.
Chemical reactivity
The presence of the chlorine and nitro group may provide the compound with chemical reactivity.
Biological activity
The indazole ring suggests potential biological activity, making 1-(3-chloro-6-nitro-1H-indazol-1-yl)ethanone of interest for further study and potential development of new materials or pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 68159-09-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,1,5 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68159-09:
(7*6)+(6*8)+(5*1)+(4*5)+(3*9)+(2*0)+(1*9)=151
151 % 10 = 1
So 68159-09-1 is a valid CAS Registry Number.
68159-09-1Relevant academic research and scientific papers
The Chemistry of 5-Oxodihydroisoxazoles. IV. Reactions of Some N-Arylisoxazol-5-ones with Nucleophiles
Ang, Kiah H.,Donati, Cosimo,Donkor, Augustine,Prager, Rolf H.
, p. 2037 - 2048 (2007/10/02)
The reactions of ethyl 2-aryl-5-oxo-2,5-dihydroisoxazole-4-carboxylate (aryl = phenyl, isoquinolin-1-yl, 2-phenylquinazolin-4-yl and 5-nitropyridin-2-yl) with azide and primary, secondary and tertiary amines, and a number of other nucleophiles are describ
