99878-79-2 Usage
Uses
Used in Pharmaceutical Research and Synthesis:
4-CHLORO-7,8-DIMETHOXYQUINOLINE is used as a chemical intermediate for the development of new pharmaceutical compounds due to its unique structure and potential therapeutic properties.
Used in Antimalarial Applications:
In the field of antimalarial research, 4-CHLORO-7,8-DIMETHOXYQUINOLINE is used as a potential antimalarial agent, given its ability to target and inhibit the growth of Plasmodium parasites, which cause malaria.
Used in Antibacterial Applications:
4-CHLORO-7,8-DIMETHOXYQUINOLINE is utilized as a potential antibacterial agent, showing promise in combating bacterial infections by interfering with essential cellular processes in bacteria.
Used in Anti-inflammatory Applications:
In the realm of anti-inflammatory research, 4-CHLORO-7,8-DIMETHOXYQUINOLINE is used as a potential anti-inflammatory agent, possibly modulating inflammatory responses and reducing inflammation-related symptoms.
Used in Antitumor Applications:
4-CHLORO-7,8-DIMETHOXYQUINOLINE is employed as a potential antitumor agent, being studied for its capacity to inhibit the growth and proliferation of tumor cells, offering a new avenue for cancer treatment.
These applications highlight the versatility and potential of 4-CHLORO-7,8-DIMETHOXYQUINOLINE in various industries, particularly in healthcare and pharmaceuticals, where its unique chemical properties are being harnessed for the development of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 99878-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,8,7 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 99878-79:
(7*9)+(6*9)+(5*8)+(4*7)+(3*8)+(2*7)+(1*9)=232
232 % 10 = 2
So 99878-79-2 is a valid CAS Registry Number.
99878-79-2Relevant academic research and scientific papers
Synthesis of the pentacyclic core of lihouidine
Feldman, Ken S.,Coca, Adiel
, p. 2136 - 2138 (2008/09/19)
The pentacyclic base of the sponge-derived alkaloid lihouidine has been assembled from two quinoline fragments. The key step is a nitration-promoted cyclization to form the C-C bond between the two quinoline units.
A SYNTHESIS OF AAPTAMINE
Kelly, T. Ross,Maguire, Martin P.
, p. 3033 - 3036 (2007/10/02)
A five-step synthesis of the unusual marine alkaloid aaptamine (1) from veratrole is described (Scheme 1).