117138-75-7 Usage
Molecular Structure
1H-Benz[g]indole-2,3-dione, 4,5-dihydro-1-(methylphenylamino)has a complex molecular structure that includes a benzindole core and a dihydro-1-(methylphenylamino) group attached to it.
Class of Compound
This chemical belongs to the class of benzindole compounds, which are known for their unique properties and potential applications in various fields.
Functional Groups
The compound contains several functional groups, including an indole ring, a dione group (C=O), a dihydro group (C-C), and a methylphenylamino group (NH).
Potential Applications
Due to its unique structure, this chemical has potential applications in pharmaceuticals and organic synthesis. It may be used in the development of new drugs or as a precursor in the synthesis of other organic compounds.
Bioactive Properties
The compound may possess bioactive properties, which could make it useful in the development of new therapeutic agents or as a target for drug design.
Further Research
To fully understand the properties and potential uses of 1H-Benz[g]indole-2,3-dione, 4,5-dihydro-1-(methylphenylamino)-, further research and analysis are necessary. This may include studying its chemical reactivity, stability, and interactions with other molecules or biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 117138-75-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,1,3 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 117138-75:
(8*1)+(7*1)+(6*7)+(5*1)+(4*3)+(3*8)+(2*7)+(1*5)=117
117 % 10 = 7
So 117138-75-7 is a valid CAS Registry Number.
117138-75-7Relevant academic research and scientific papers
REACTIONS WITH CYCLIC OXALYL COMPOUNDS, PART 26: THE FISCHER-INDOLE REARRANGEMENT OF STERICALLY HINDERED SYSTEMS, PART 7: DIAZA PROPELLANES VIA THERMALLY INITIATED FISCHER-INDOLIZATION
Kollenz, Gert,Theuer, Ralph,Ott, Walter,Peters, Karl,Peters, Eva-Maria,Schnering, Hans Georg von
, p. 479 - 494 (2007/10/02)
The 4,5-bridged pyrrol-2,3-diones 3, obtained from cyclocondensation reactions of the N,N-disubstituted hydrazones 2 and oxalyl dichloride, can be rearranged into the corresponding diaza propellanes 4 via a thermally initiated Fischer-indolization process.Their molecular structure is confirmed with aid of an X-ray structure determination of 4a and chemical degradation reactions leading to the tetracyclic indole systems 5.
