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ChemicalBook >> CAS DataBase List >>4-Chloroquinoline-6-carboxylic acid ethyl ester

4-Chloroquinoline-6-carboxylic acid ethyl ester

CAS No.
148018-34-2
Chemical Name:
4-Chloroquinoline-6-carboxylic acid ethyl ester
Synonyms
CAS:148018-34-2;Ethyl 4-chloro-6-quinolinecarboxylate;ethyl 4-chloroquinoline-6-carboxylate;4-Chloroquinoline-6-carboxylic acid ethyl ester;6-Quinolinecarboxylic acid, 4-chloro-, ethyl ester
CBNumber:
CB22511504
Molecular Formula:
C12H10ClNO2
Molecular Weight:
235.67
MDL Number:
MFCD16250588
MOL File:
148018-34-2.mol
Last updated:2025-07-24 18:13:44

4-Chloroquinoline-6-carboxylic acid ethyl ester Properties

storage temp. under inert gas (nitrogen or Argon) at 2-8°C
Appearance White to off-white Solid

4-Chloroquinoline-6-carboxylic acid ethyl ester price More Price(15)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation HCH0368892 ETHYL-4-CHLOROQUINOLINE-6-CARBOXYLATE 95.00% 148018-34-2 5MG $499.44 2021-12-16 Buy
American Custom Chemicals Corporation HCH0368892 ETHYL-4-CHLOROQUINOLINE-6-CARBOXYLATE 95.00% 148018-34-2 1G $982.8 2021-12-16 Buy
Labseeker SC-44820 4-Chloroquinoline-6-carboxylicacidethylester 95 148018-34-2 2g $1166 2021-12-16 Buy
Chemenu CM144480 ethyl4-chloroquinoline-6-carboxylate 97% 148018-34-2 5g $1636 2021-12-16 Buy
Alichem 148018342 Ethyl4-chloroquinoline-6-carboxylate 148018-34-2 5g $1663.45 2021-12-16 Buy
Product number Packaging Price Buy
HCH0368892 5MG $499.44 Buy
HCH0368892 1G $982.8 Buy
SC-44820 2g $1166 Buy
CM144480 5g $1636 Buy
148018342 5g $1663.45 Buy

4-Chloroquinoline-6-carboxylic acid ethyl ester Chemical Properties,Uses,Production

Synthesis

4-Oxo-1,4-dihydro-quinoline-6-carboxylic acid ethyl ester

127286-04-8

4-Chloroquinoline-6-carboxylic acid ethyl ester

148018-34-2

The general procedure for the synthesis of ethyl 4-chloroquinoline-6-carboxylate from the compound (CAS:127286-04-8) was as follows: intermediate 41 (3 g, 13.8 mmol) was mixed with phosphorus trichloride (8 mL) and the reaction was stirred at 120 °C for 3 hours. Upon completion of the reaction, the solvent was removed by vacuum evaporation and subsequently quenched by adding crushed ice to the residue. Next, saturated aqueous sodium bicarbonate solution with ethyl acetate was added to the mixture to form a two-phase system. The organic and aqueous phases were separated and the aqueous phase was then extracted with ethyl acetate. All organic phases were combined, dried with anhydrous sodium sulfate, filtered to remove the desiccant, and the filtrate was evaporated under vacuum to remove the volatile components. Finally, the target product ethyl 4-chloroquinoline-6-carboxylate (2.19 g, 67% yield) was purified by silica gel column chromatography.

References

[1] Patent: US2008/234267, 2008, A1. Location in patent: Page/Page column 25

148018-33-1
148018-34-2
Synthesis of 4-Chloroquinoline-6-carboxylic acid ethyl ester from Ethyl 4-hydroxyquinoline-6-carboxylate

4-Chloroquinoline-6-carboxylic acid ethyl ester Preparation Products And Raw materials

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4-Chloroquinoline-6-carboxylic acid ethyl ester Spectrum

4-Chloroquinoline-6-carboxylic acid ethyl ester ethyl 4-chloroquinoline-6-carboxylate Ethyl 4-chloro-6-quinolinecarboxylate 6-Quinolinecarboxylic acid, 4-chloro-, ethyl ester CAS:148018-34-2 148018-34-2