Interesting facts
Interesting Facts about Ethyl 6-decoxy-7-ethoxy-4-oxo-1H-quinoline-3-carboxylate
Ethyl 6-decoxy-7-ethoxy-4-oxo-1H-quinoline-3-carboxylate is a fascinating compound that falls within the realm of quinoline derivatives, renowned for their diverse range of biological activities. Quinoline compounds, in general, have intrigued scientists due to their role in medicinal chemistry and organic synthesis.
Key Highlights:
- Biological Activity: Quinoline derivatives, including this compound, are often explored for their potential antimicrobial, antimalarial, and anticancer activities, making them important in the field of drug discovery.
- Synthetic Versatility: The unique structure of quinolines allows for various chemical modifications, which can unleash different therapeutic properties and broaden their application spectra.
- Research Applications: Compounds like ethyl 6-decoxy-7-ethoxy-4-oxo-1H-quinoline-3-carboxylate are valuable in studies related to enzyme inhibition and receptor interaction, giving insights into complex biological processes.
- Quinoline Core: The quinoline skeleton itself is noteworthy since it can facilitate the formation of various heterocycles that are foundational to many natural products and pharmaceuticals.
As we delve deeper into the properties and functionalities of ethyl 6-decoxy-7-ethoxy-4-oxo-1H-quinoline-3-carboxylate, one can't help but appreciate the intricate balance between structure and activity that defines this compound and its potential applications in the realm of chemistry and medicine. The journey towards understanding such compounds not only enhances our chemical knowledge but also serves as a stepping stone towards innovative therapeutic modalities.
Synonyms
DECOQUINATE
18507-89-6
Deccox
HC 1528
Decoquinato
Decoquinatum
M&B 15497
3-Quinolinecarboxylic acid, 6-(decyloxy)-7-ethoxy-4-hydroxy-, ethyl ester
NSC-339057
534I52PVWH
DTXSID5046851
HC-1528
DTXCID3026851
M&B-15497
Deccox M
Ethyl-6-(Decycloxy)-7-ethoxy-4-hydroxy-3-quinolinecarboxylate
Deccox-M Medicated Powder for Whole Milk
6-decoxy-7-ethoxy-4-oxo-1H-quinoline-3-carboxylic acid ethyl ester
ethyl 6-(decyloxy)-7-ethoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate
Decoxy
Ethyl 6-(decyloxy)-7-ethoxy-4-hydroxyquinoline-3-carboxylate
ethyl 6-decoxy-7-ethoxy-4-oxo-1H-quinoline-3-carboxylate
NSC 339057
MFCD00673686
Ethyl 6-(decyloxy)-7-ethoxy-4-hydroxy-3-quinolinecarboxylate
M and B 15497
NSC339057
NCGC00181109-01
Decoquinate 100 microg/mL in Acetonitrile/DMF
Decoquinatum [INN-Latin]
Decoquinato [INN-Spanish]
CAS-18507-89-6
EINECS 242-389-1
Ethyl 6-decyloxy-7-ethoxy-4-hydroxy-3-quinolinate
UNII-534I52PVWH
Decoquinat
DeccoxTM
Decoquinate [USAN:USP:INN:BAN]
Deccox (TN)
Ethyl 5-decyloxy-7-ethoxy-4-hydroxy-3-chinolincarboxylat
Decoquinate (Standard)
Decoquinate (USP/INN)
DECOQUINATE [MI]
DECOQUINATE [INN]
DECOQUINATE [USAN]
DECOQUINATE [MART.]
SCHEMBL43853
SCHEMBL43854
DECOQUINATE [USP-RS]
CHEMBL416230
orb1310580
DECOQUINATE [GREEN BOOK]
M. and B. 15497
SCHEMBL29373625
HY-B1036R
Ethyl 6-decyloxy-7-ethoxy-4-hydroxy-3-quinolinecarboxylate
Ethyl 6-Decyloxy-7-ethoxy-4-hydroxyquinoline-3-carboxylate
MSK5710
HMS2093D11
Pharmakon1600-01505356
DECOQUINATE [USP MONOGRAPH]
BCP28448
ethyl 6-(n-decyloxy)-7-ethoxy-4-hydroxyquinoline-3-carboxylate
HY-B1036
Tox21_112723
NSC759109
s4145
AKOS015895953
AKOS022185844
DECOQUINATE, REFERENCE STANDARD
Tox21_112723_1
CS-4555
DB11394
FD20875
NSC-759109
NCGC00181109-03
NCGC00264109-01
AS-13953
SY052969
SBI-0206843.P001
DB-065512
D4192
NS00010345
D03667
F21439
F90392
AB01563292_01
AB01563292_02
Decoquinate, VETRANAL(TM), analytical standard
SR-05000001968
Q5249594
SR-05000001968-1
BRD-K17641316-001-01-4
BRD-K17641316-001-02-2
BRD-K17641316-001-03-0
BRD-K17641316-001-04-8
BRD-K17641316-213-01-5
ethyl 6-decoxy-7-ethoxy-4-hydroxy-quinoline-3-carboxylate
Decoquinate, United States Pharmacopeia (USP) Reference Standard
6-Decyloxy-7-ethoxy-4-hydroxy-3-quinolinecarboxylic acid ethyl ester
6-Decyloxy-7-ethoxy-4-hydroxyquinoline-3-carboxylic Acid Ethyl Ester
6-(Decyloxy)-7-ethoxy-4-hydroxy3-quinolinecarboxylic acid ethyl ester;Deccox;Decoxy
Solubility of Ethyl 6-decoxy-7-ethoxy-4-oxo-1H-quinoline-3-carboxylate
The solubility of ethyl 6-decoxy-7-ethoxy-4-oxo-1H-quinoline-3-carboxylate can be described as being influenced by its complex molecular structure. Understanding its solubility characteristics is crucial for various applications, including pharmaceutical formulations and chemical processes.
Generally, quinoline derivatives tend to exhibit a range of solubility behaviors. Here are some factors affecting the solubility of this compound:
In conclusion, while ethyl 6-decoxy-7-ethoxy-4-oxo-1H-quinoline-3-carboxylate may show moderate solubility in certain organic solvents, its solubility behavior is complex and is highly influenced by the factors mentioned above. Therefore, thorough evaluation is necessary to understand its practical applications.