1233-49-4 Usage
Uses
Used in Pharmaceutical Industry:
INDOLE-3-ALDEHYDE AZINE is used as a building block for the synthesis of novel compounds with potential medicinal applications. Its unique structure and properties make it a valuable component in the development of new drugs.
Used in Chemical Research:
INDOLE-3-ALDEHYDE AZINE is used as a research chemical to study the biological activities of indole-based compounds. This helps in understanding their potential applications and mechanisms of action in various biological processes.
Used in Drug Development:
INDOLE-3-ALDEHYDE AZINE may have potential applications in the development of new drugs due to its unique properties and ability to be incorporated into novel compound structures. Its study and synthesis can contribute to the discovery of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 1233-49-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,3 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1233-49:
(6*1)+(5*2)+(4*3)+(3*3)+(2*4)+(1*9)=54
54 % 10 = 4
So 1233-49-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H14N4/c1-3-7-17-15(5-1)13(9-19-17)11-21-22-12-14-10-20-18-8-4-2-6-16(14)18/h1-12,21-22H
1233-49-4Relevant academic research and scientific papers
Shiraishi, Yasuhiro,Maehara, Hajime,Hirai, Takayuki
, p. 2072 - 2076 (2009)
An indole-azadiene conjugate (1), synthesized by facile one-step condensation, behaves as a highly selective probe for detection of fluoride ion both in colorimetric and fluorometric analyses. The probe 1 shows F --selective color change from colorless to yellow and appearance of green fluorescence. 1H NMR analysis and ab initio calculation reveal that the F--induced colorimetric and fluorometric responses of 1 are simply driven by hydrogen bonding interaction between the indolic NH protons and F-.
Synthesis and X-ray Photoelectron Spectra of Some Azines
El-Rayyes, Nizar R.,Katrib, Ali H.
, p. 132 - 134 (2007/10/02)
Arylhydrazone-N-carboxylic esters (I) were treated with hydrazine hydrate, or sodium hydroxide, to give the hydrazones (II).Acidification of the latter produced the corresponding azines (III).The structures of compounds I - III were substantiated by chemical and spectral analysis.
