92592-31-9 Usage
Explanation
This is the chemical name of the compound, which describes its structure and components.
Explanation
The compound is used in the field of pharmaceuticals for research and development of potential drugs.
3. Derivative of indole
Explanation
The compound is derived from indole, a heterocyclic compound consisting of a benzene ring fused to a pyrrole ring.
4. Potential bioactive properties
Explanation
The compound may have biological activities, such as interacting with biological systems or organisms.
5. Nitrile group presence
Explanation
The molecule contains a nitrile group (C≡N), which may contribute to its potential biological activities.
6. Keto group presence
Explanation
The molecule also contains a keto group (C=O), which can further influence its biological activities.
7. Antiviral, antibacterial, or antifungal properties
Explanation
The presence of a nitrile group and a keto group suggests that the compound may exhibit activities against viruses, bacteria, or fungi.
8. Precursor in organic synthesis
Explanation
The compound's molecular structure indicates that it may serve as a starting material or intermediate in the synthesis of other organic compounds.
9. Further research needed
Explanation
More research is required to fully understand the potential uses and applications of this chemical compound.
Usage
Pharmaceutical research and development
Check Digit Verification of cas no
The CAS Registry Mumber 92592-31-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,5,9 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 92592-31:
(7*9)+(6*2)+(5*5)+(4*9)+(3*2)+(2*3)+(1*1)=149
149 % 10 = 9
So 92592-31-9 is a valid CAS Registry Number.
92592-31-9Relevant academic research and scientific papers
Ketene. Part 21. Reactions of Heterocumulenes with Nitrones
Evans, Andrew R.,Hafiz, Mushtaq,Taylor, Giles A.
, p. 1241 - 1246 (2007/10/02)
Degradative and mass spectrometric evidence confirms the formation of the isoxazolidinones (2) from the reaction of cyano-t-butylketene with the N-alkyl nitrones (1), whilst the reaction with the N-phenyl nitrone (1d) gives the expected oxazolidinone (3b).Cyano-t-butylketene reacts with diphenyl nitrone to give the indolones (10a) and (10b).The reaction of phenyl isocyanate with diphenyl nitrone, and the N-alkyl nitrones (1a) and (1d) gives the normal 1,3-dipolar cycloadducts without rearrangement.Ethoxycarbonyl-t-butylketene reacts with the N-phenyl nitrone (1d) to give an oxazolidinone , but reaction with the N-alkyl nitrones (1) gives only fluorenone azine.This ketene reacts with diphenyl nitrone to give the anil (15) and the dihydroindole (16).
