300587-41-1 Usage
Uses
Used in Pharmaceutical Research:
4,5-Dihydro[1,2,5]oxadiazolo[3,4-f]cinnoline is used as a scaffold for the design of novel therapeutic compounds, owing to its unique structure and potential for the development of new drugs.
Used in Cancer Treatment:
In the field of oncology, 4,5-dihydro[1,2,5]oxadiazolo[3,4-f]cinnoline is used as an anti-cancer agent. Its complex structure allows for the exploration of its potential in targeting and treating various types of cancer.
Used in Neuroprotection:
4,5-Dihydro[1,2,5]oxadiazolo[3,4-f]cinnoline also shows promise as a neuroprotective agent, indicating its potential use in the development of treatments for neurological disorders and conditions.
Further research is necessary to fully understand the properties and potential applications of 4,5-dihydro[1,2,5]oxadiazolo[3,4-f]cinnoline, as its complex structure and potential uses span across various fields in medicine and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 300587-41-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,0,5,8 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 300587-41:
(8*3)+(7*0)+(6*0)+(5*5)+(4*8)+(3*7)+(2*4)+(1*1)=111
111 % 10 = 1
So 300587-41-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N4O/c1-2-7-8(12-13-11-7)5-3-4-9-10-6(1)5/h3-4H,1-2H2
300587-41-1Relevant academic research and scientific papers
Formation of the pyrroline N-oxide ring by interaction of α-isonitrosoketones-derivatives of tetrahydrobenzofurazan and -furoxan with aldehydes and morpholine and some of the reactions of these compounds
Samsonov
, p. 1346 - 1351 (2007/10/03)
α-Isonitroso ketones, derivatives of tetrahydrobenzofurazan and furoxan, react with aldehydes (acetaldehyde and propionaldehyde) and morpholine to form derivatives of tetrahydropyrrolo[2,3-e]-2,1,3-benzoxadiazole 6-oxide. Treatment of the latter with hydrazine hydrate gave derivatives of 4,5-dihydro-1,2,5-oxadiazolo[3,4-f]cinnoline which are readily dehydrogenated with tetrachloro-benzoquinone to derivatives of 1,2,5-oxadiazolo[3,4-f] cinnoline. Reduction of tetrahydropyrrolo[2,3-e]-2,1,3-benzoxadiazole 6-oxides with sodium borohydride gave derivatives of N-hydroxyhexahydro-pyrrolo[2,3-e]-2, 1,3-benzoxazole.
