57102-97-3 Usage
Uses
Used in Organic Synthesis:
N-ETHYL-6-BROMO-CARBAZOLE is used as a starting material for the synthesis of other organic compounds, contributing to the development of new chemical entities with diverse applications.
Used in Materials Science:
In the field of materials science, N-ETHYL-6-BROMO-CARBAZOLE is employed for its properties that can enhance or modify the characteristics of various materials, potentially improving their performance in different applications.
Used in Pharmaceutical Industry:
N-ETHYL-6-BROMO-CARBAZOLE is used as an intermediate in the pharmaceutical industry for the development of new drugs, leveraging its chemical structure to create novel therapeutic agents.
Used in OLEDs Manufacturing:
N-ETHYL-6-BROMO-CARBAZOLE is used as a component in the manufacture of OLEDs (organic light-emitting diodes) for its ability to contribute to the light-emitting properties of these devices, enhancing their efficiency and performance in display and lighting technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 57102-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,1,0 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 57102-97:
(7*5)+(6*7)+(5*1)+(4*0)+(3*2)+(2*9)+(1*7)=113
113 % 10 = 3
So 57102-97-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H12BrN/c1-2-16-13-6-4-3-5-11(13)12-9-10(15)7-8-14(12)16/h3-9H,2H2,1H3
57102-97-3Relevant academic research and scientific papers
A new method for bromination of carbazoles, β-carbolines and iminodibenzyls by use of N-bromosuccinimide and silica gel
Smith, Keith,Martin James,Mistry, Anil G.,Bye, Martin R.,John Faulkner
, p. 7479 - 7488 (2007/10/02)
Carbazole, N-ethylcarbazole, iminodibenzyl (10,11-dihydro-5H-dibenz[b,f]azepine), N-ethyliminodibenzyl and imipramine are readily mono-, di- or polybrominated in high yields at ambient temperature in dichloromethane by use of the appropriate quantity of N-bromosuccinimide in the presence of silica gel. By contrast, the brominations of the β-carbolines, harmane and norharman, are less selective and give mixtures of products, some of which have unusual substitution patterns.
