550612
Ethyl 3-quinolinecarboxylate
97%
Synonym(s):
Quinoline-3-carboxylic acid ethyl ester
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C12H11NO2
CAS Number:
Molecular Weight:
201.22
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
97%
bp
120 °C/0.4 mmHg (lit.)
mp
63-67 °C (lit.)
functional group
ester
SMILES string
CCOC(=O)c1cnc2ccccc2c1
InChI
1S/C12H11NO2/c1-2-15-12(14)10-7-9-5-3-4-6-11(9)13-8-10/h3-8H,2H2,1H3
InChI key
OTTDACPMYLDVTL-UHFFFAOYSA-N
General description
Ethyl 3-quinolinecarboxylate can be prepared from 3-quinolinecarboxylic acid by treating with thionyl chloride followed by esterification with ethanol. Its photochemical reaction in various alcohols and cyclohexane show that the nature of the solvent has an impact on the product formation.[1]
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Photochemical reactions of ethoxycarbonyl-substituted quinolines.
Ono I and Hata N.
Bulletin of the Chemical Society of Japan, 60(8), 2891-2897 (1987)
QUINOLINEMETHANOLS1.
Kaslow CE and Clark WR.
The Journal of Organic Chemistry, 18(1), 55-58 (1953)
Biosynthesis of Penicillins. VI. N-2-Hydroxyethylamides of Some Polycyclic and Heterocyclic Acetic Acids as Precursors1.
Jones RG, et al.
Journal of the American Chemical Society, 70(9), 2843-2848 (1948)
Active Filters
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service
