30727-61-8 Usage
Description
6-bromobenzo[h]quinoline is a chemical compound belonging to the benzoquinoline family, characterized by a molecular formula of C13H8BrN. It features a benzene ring fused to a quinoline ring, with a bromine atom attached at the 6th position of the benzene ring. 6-bromobenzo[h]quinoline is recognized for its significance in organic synthesis and medicinal chemistry, where it serves as a building block for creating various pharmaceuticals and bioactive molecules. Additionally, 6-bromobenzo[h]quinoline exhibits potential therapeutic applications, particularly in the realms of anticancer and antimicrobial treatments. Its chemical structure and reactivity contribute to its value in the development of innovative drugs and biologically active compounds.
Uses
Used in Organic Synthesis:
6-bromobenzo[h]quinoline is utilized as a key intermediate in organic synthesis for the preparation of a range of pharmaceuticals and bioactive molecules. Its unique structure and reactivity make it a versatile component in the creation of complex organic compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 6-bromobenzo[h]quinoline is employed as a building block for the development of new drugs. Its chemical properties allow for the design and synthesis of molecules with potential therapeutic effects.
Used in Anticancer Applications:
6-bromobenzo[h]quinoline is recognized for its potential as an anticancer agent. It is being explored for its ability to target and treat various types of cancer, offering a promising avenue for cancer therapy.
Used in Antimicrobial Applications:
6-bromobenzo[h]quinoline also demonstrates potential in antimicrobial applications, where it can be used to combat microbial infections. Its effectiveness against certain microorganisms positions it as a candidate for further research and development in the field of antimicrobial agents.
Used in Drug Development:
6-bromobenzo[h]quinoline is a valuable tool in drug development, where its chemical structure and reactivity are leveraged to create new and effective biologically active compounds. Its role in this process is crucial for advancing the discovery and creation of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 30727-61-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,7,2 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 30727-61:
(7*3)+(6*0)+(5*7)+(4*2)+(3*7)+(2*6)+(1*1)=98
98 % 10 = 8
So 30727-61-8 is a valid CAS Registry Number.
30727-61-8Relevant articles and documents
Synthesis of benzoquinoline derivatives from formyl naphthylamines via Friedl?nder annulation under metal-free conditions
Malinowski, Zbigniew,Fornal, Emilia,Warpas, Anna,Nowak, Monika
, p. 1999 - 2011 (2018/09/25)
Abstract: The synthesis of benzoquinolines and benzoquinolinones via Friedl?nder-type condensation of aminonaphthalene carbaldehydes with (1) primary or secondary alcohols mediated by urea/KOH or with (2) diketones or β-ketoesters is described. The behavi
