67618-28-4 Usage
Uses
Used in Organic Synthesis:
(1E)-N-methyl-1-(methylimino)-1H-phenalen-9-amine is utilized as a reactant or catalyst in various organic synthesis reactions. Its unique structure and reactivity contribute to the formation of new compounds and the enhancement of reaction efficiency.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, (1E)-N-methyl-1-(methylimino)-1H-phenalen-9-amine serves as a key component in the development of innovative drugs and medical treatments. Its potential applications in this field highlight its importance in creating novel therapeutic agents.
Used in Academic Research:
Due to its distinctive chemical properties, (1E)-N-methyl-1-(methylimino)-1H-phenalen-9-amine is also employed in academic research. It aids scientists in understanding complex chemical reactions and contributes to the advancement of chemical knowledge.
Used in Chemical Analysis:
(1E)-N-methyl-1-(methylimino)-1H-phenalen-9-amine's unique structure and reactivity make it a valuable tool in chemical analysis. It can be used to study and identify specific chemical interactions and processes, further expanding its utility in the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 67618-28-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,6,1 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 67618-28:
(7*6)+(6*7)+(5*6)+(4*1)+(3*8)+(2*2)+(1*8)=154
154 % 10 = 4
So 67618-28-4 is a valid CAS Registry Number.
67618-28-4Relevant academic research and scientific papers
Mandal, Swadhin K.,Itkis, Mikhail E.,Chi, Xiaoliu,Samanta, Satyabrata,Lidsky, David,Reed, Robert W.,Oakley, Richard T.,Tham, Fook S.,Haddon, Robert C.
, p. 8185 - 8196 (2005)
We report the preparation, crystallization, and solid-state characterization of the first members of a new family of spiro-bis-(1,9-diamino- substituted-phenalenyl)boron neutral radicals. The crystal structures show that the three radicals are monomeric a
1,9-Disubstituted phenalenes-I. Synthesis of n- and s-derivatives of 9-hydroxy-1-phenalenone
Franz,Martin
, p. 2147 - 2151 (2007/10/06)
The reaction of 9-hydroxy-1-phenalenone with Ag2O and alkyliodides gives the analogous β-keto-ethers from which synthetic pathways have been devised to isolate and characterise some nitrogen and sulphur derivatives. As intermediates stable phenalenium cations can be isolated by the reaction of 9-substituted 1-phenalenones with [(C2H5)3O]+BF4-. Whenever possible, a strong intramolecular H-bond is formed between the 1-and 9-substituents as shown by the low-field resonances of the respective hydrogens in the 1H NMR and the stability of the compounds towards reduction.
