272776-07-5 Usage
Uses
Used in Pharmaceutical Development:
9-METHYL[1,2,5]OXADIAZOLO[3,4-F]CINNOLINE is used as a pharmacological agent for its potential role in medicinal chemistry and drug development. Its unique molecular structure and properties make it a candidate for the development of novel pharmaceuticals that could address various medical conditions.
Used in Materials Science:
In the field of materials science, 9-METHYL[1,2,5]OXADIAZOLO[3,4-F]CINNOLINE is used for its potential applications in creating new materials with specific properties, leveraging its unique chemical structure.
Used in Chemical Synthesis:
9-METHYL[1,2,5]OXADIAZOLO[3,4-F]CINNOLINE is utilized as a key intermediate in chemical synthesis processes, where its distinctive structure can contribute to the creation of new chemical entities with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 272776-07-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,2,7,7 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 272776-07:
(8*2)+(7*7)+(6*2)+(5*7)+(4*7)+(3*6)+(2*0)+(1*7)=165
165 % 10 = 5
So 272776-07-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H6N4O/c1-5-4-10-11-6-2-3-7-9(8(5)6)13-14-12-7/h2-4H,1H3
272776-07-5Relevant 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.
