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Ethyl 2-ethoxyquinoline-1-carboxylate

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Identification
Molecular formula
C14H15NO3
CAS number
622-96-8
IUPAC name
ethyl 2-ethoxy-2H-quinoline-1-carboxylate
State
State

At room temperature, ethyl 2-ethoxyquinoline-1-carboxylate is in a solid state. It forms a stable crystalline structure under standard atmospheric conditions.

Melting point (Celsius)
79.00
Melting point (Kelvin)
352.15
Boiling point (Celsius)
377.40
Boiling point (Kelvin)
650.50
General information
Molecular weight
247.28g/mol
Molar mass
247.2790g/mol
Density
1.1120g/cm3
Appearence

Ethyl 2-ethoxyquinoline-1-carboxylate is typically a crystalline solid with a white to off-white appearance. The compound may form powder or small crystal formations depending on its purity and preparation method.

Comment on solubility

Solubility of Ethyl 2-ethoxy-2H-quinoline-1-carboxylate

Ethyl 2-ethoxy-2H-quinoline-1-carboxylate is an intriguing compound when considering its solubility profile. Generally, the solubility of organic compounds is influenced by molecular structure and interactions with solvents.

Key Factors Affecting Solubility:

  • Polarity: Ethyl 2-ethoxy-2H-quinoline-1-carboxylate contains ethoxy and quinoline groups which can impart varying degrees of polarity, affecting how well it dissolves in polar versus non-polar solvents.
  • Functional Groups: The presence of the carboxylate group could offer some hydrogen bonding opportunities, which enhances solubility in polar solvents.
  • Temperature: As with many organic compounds, increasing the temperature often increases solubility, particularly in organic solvents.

In general, this compound is expected to be more soluble in organic solvents like ethanol or acetone rather than in water. Understanding the solubility of ethyl 2-ethoxy-2H-quinoline-1-carboxylate can play a crucial role in its applications in various chemical reactions and formulations.

While "like dissolves like" is a common rule in chemistry, the specific solubility characteristics of this compound warrant further investigation, particularly for practical uses in different solvents.

Interesting facts

Interesting Facts about Ethyl 2-Ethoxy-2H-Quinoline-1-Carboxylate

Ethyl 2-ethoxy-2H-quinoline-1-carboxylate is an intriguing compound that belongs to the class of quinolines, known for their diverse biological activities and applications in medicinal chemistry. This compound is notable for its unique chemical structure and properties, making it a subject of interest across various fields of research. Here are some fascinating insights:

  • Structural Versatility: The presence of the ethoxy group and the carboxylate functionality in its structure allows for various chemical modifications, enabling scientists to explore a range of derivatives with potentially enhanced activities.
  • Biological Activity: Compounds featuring quinoline moieties, such as ethyl 2-ethoxy-2H-quinoline-1-carboxylate, have been studied for various pharmacological activities, including antimalarial, antimicrobial, and anticancer properties.
  • Synthesis Techniques: The synthesis of this compound often involves innovative methods, including multicomponent reactions that showcase the versatility of organic chemistry in creating complex molecules from simpler starting materials.
  • Research Applications: Due to its quinoline backbone, this compound holds promising implications in drug discovery and development, particularly in the search for new therapies against resistant microbial strains.

As researchers continue to unravel the potential of ethyl 2-ethoxy-2H-quinoline-1-carboxylate, its role could expand within the realms of medicinal chemistry and materials science, affirming the significance of exploring quinoline derivatives and their impact on modern scientific advancements.

Synonyms
16357-59-8
EEDQ
1(2H)-QUINOLINECARBOXYLIC ACID, 2-ETHOXY-, ETHYL ESTER
2-Ethoxy-1(2H)-quinolinecarboxylic acid, ethyl ester
N-carbethoxy-2-ethoxy-1,2-dihydroquinoline
60O971AN19
DTXSID50871969
2-ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline
DTXCID40819577
2-Ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline
N-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline
ethyl 2-ethoxyquinoline-1(2H)-carboxylate
ethyl 2-ethoxy-2H-quinoline-1-carboxylate
MFCD00006703
1-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline
ethyl 2-ethoxy-1,2-dihydroquinoline-1-carboxylate
BC 681
NSC 147831
MLS000069601
SMR000059033
2-Ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline (EEDQ)
Ethyl 2-ethoxy-1(2H)-quinolinecarboxylate
NSC-147831
2-ethoxy-N-ethoxycarbonyl-1,2-dihydroquinoline
2-ethoxy-n-(ethoxycarbonyl)-1,2-dihydroquinoline
ethyl 2-ethoxy-1,2-dihydroquinolinecarboxylate
EINECS 240-418-2
BRN 0533048
UNII-60O971AN19
ethyl 1,2-dihydro-2-ethoxy-1-quinolinecarboxylate
Ethyl N-(2-ethoxy-1,2-dihydroquinoline)carboxylate
Opera_ID_1846
SCHEMBL338
EEDQ [MI]
1-ethoxycarbonyl-2-ethoxy-1
5-21-03-00028 (Beilstein Handbook Reference)
cid_27833
Ethyl 1,2-dihydro-2-ethoxyquinoline-1-carboxylate
2-ethoxy-1(2H)-quinolinecarboxylic acid ethyl ester
orb1737571
SCHEMBL6765651
SCHEMBL6765653
CHEMBL1527785
SCHEMBL29367804
BDBM40545
GKQLYSROISKDLL-UHFFFAOYSA-
HMS1776O14
HY-Y1191
BBL011113
BC-681
NSC147831
SBB057548
STK802369
WLN: T66 BN CHJ BVO2 CO2
AKOS001075463
AKOS016842289
AC-2881
FE40640
SB40704
NCGC00246989-01
AS-15469
BP-24399
ethyl2-ethoxyquinoline-1(2H)-carboxylate
SY003226
1-carbethoxy-2-ethoxy-1,2-dihydroquinoline
1-carbethoxy-2-ethoxy-l,2-dihydroquinoline
DB-019159
CS-0017180
E0363
NS00054945
ST50308466
2-ethoxy-1-ethoxycarbonyl-1,2dihydroquinoline
EN300-18587
1-ethoxycabonyl-2-ethoxy-1,2-dihydroquinoline
2-ethoxy-1-ethoxycarbonyl-1,2-dihydrochinolin
2-ethoxy-1-ethoxycarbonyl-1.2-dihydroquinoline
2-ethoxy-l-ethoxycarbonyl-1,2-dihydroquinoline
E-5001
P16694
2-ethyoxy-1-ethoxycarbonyl-1,2-dihydroquinoline
Ethyl 2-ethoxy-1,2-dihydro-1-quinolinecarboxylate
2-ethoxy-2h-quinoline-1-carboxylic acid ethyl ester
2-ethoxy- 1(2H)-quinolinecarboxylic acid ethyl ester
Q10859667
Z85921046
2-Ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline, >=99%
F0001-0593
(3Z)-3-(ethoxy-hydroxymethylidene)-1-methylquinoline-2,4-dione
InChI=1/C14H17NO3/c1-3-17-13-10-9-11-7-5-6-8-12(11)15(13)14(16)18-4-2/h5-10,13H,3-4H2,1-2H3