5416-22-8 Usage
Uses
Used in Organic Synthesis:
3,6-Dibromo-1-nitro-9H-carbazole is used as a building block in the synthesis of organic compounds, particularly for the creation of new molecules with specific properties and functions.
Used in Materials Science:
In the field of materials science, 3,6-Dibromo-1-nitro-9H-carbazole is utilized for its potential applications in developing novel materials with unique characteristics, such as improved stability or specific optical, electronic, or mechanical properties.
Used in Pharmaceutical Research:
3,6-Dibromo-1-nitro-9H-carbazole serves as a valuable compound in pharmaceutical research, where it may contribute to the discovery and development of new drugs with therapeutic potential.
Used as a Chemical Reaction Reagent:
3,6-Dibromo-1-nitro-9H-carbazole may also be used as a reagent in certain chemical reactions for the introduction of specific functional groups, which can be crucial for the synthesis of complex organic molecules or for modifying existing compounds to enhance their properties or reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 5416-22-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5416-22:
(6*5)+(5*4)+(4*1)+(3*6)+(2*2)+(1*2)=78
78 % 10 = 8
So 5416-22-8 is a valid CAS Registry Number.
5416-22-8Relevant academic research and scientific papers
Filimonov,Kulmanakova,Yusubov,Perederina,Chi, Ki-Whan,Poleshchuk
, p. 917 - 923 (2004)
Alkali metal halides NaF, KCl, and KBr sharply enhance the nitrating activity of sodium nitrate in acetic acid with respect to 9-methylcarbazole. In the presence of KI and KBr, both nitration and halogenation of the substrate occurs, while KCl and NaF promote only the nitration process. The results may be interpreted in terms of formation of the corresponding nitryl halides XNO2 (X = F, Cl, Br, I) whose structure and reactivity were examined in the framework of the density functional theory (DFT B3LYP/3-21G*).
