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ETHYL 2-(QUINOLIN-6-YL)ACETATE is a chemical compound belonging to the quinoline family, which are nitrogen-containing compounds extensively utilized in medicinal chemistry. It features a quinoline ring connected to an acetate group, with an ethyl group attached to the acetate. ETHYL 2-(QUINOLIN-6-YL)ACETATE is soluble in various common organic solvents and is primarily used in scientific research, particularly for investigating the properties and reactions of similar chemical structures. Due to its chemical nature, it is essential to handle ETHYL 2-(QUINOLIN-6-YL)ACETATE with caution to minimize potential health risks associated with exposure.

5622-38-8

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5622-38-8 Usage

Uses

Used in Scientific Research:
ETHYL 2-(QUINOLIN-6-YL)ACETATE is used as a research compound for exploring the properties and reactions of quinoline-based structures. Its application in this context aids in understanding the behavior of related chemical compounds and their potential applications in medicinal chemistry.
Used in Medicinal Chemistry:
ETHYL 2-(QUINOLIN-6-YL)ACETATE is used as a chemical intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity make it a valuable component in the development of new drugs and therapeutic agents.
Used in Chemical Synthesis:
ETHYL 2-(QUINOLIN-6-YL)ACETATE is used as a reagent in the synthesis of complex organic molecules. Its versatility in reacting with other compounds allows for the creation of a wide range of chemical products, which can be further utilized in various industries and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 5622-38-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,2 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5622-38:
(6*5)+(5*6)+(4*2)+(3*2)+(2*3)+(1*8)=88
88 % 10 = 8
So 5622-38-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H13NO2/c1-2-16-13(15)9-10-5-6-12-11(8-10)4-3-7-14-12/h3-8H,2,9H2,1H3

5622-38-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 2-(quinolin-6-yl)acetate

1.2 Other means of identification

Product number -
Other names ethyl 2-quinolin-6-ylacetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5622-38-8 SDS

5622-38-8Downstream Products

5622-38-8Relevant academic research and scientific papers

Copper-Catalyzed Ullmann-Type Coupling and Decarboxylation Cascade of Arylhalides with Malonates to Access α-Aryl Esters

Cheng, Fei,Chen, Tao,Huang, Yin-Qiu,Li, Jia-Wei,Zhou, Chen,Xiao, Xiao,Chen, Fen-Er

supporting information, p. 115 - 120 (2022/01/04)

We have developed a high-efficiency and practical Cu-catalyzed cross-coupling to directly construct versatile α-aryl-esters by utilizing readily available aryl bromides (or chlorides) and malonates. These gram-scale approaches occur with turnovers of up to 1560 and are smoothly conducted by the usage of a low catalyst loading, a new available ligand, and a green solvent. A variety of functional groups are tolerated, and the application occurs with α-aryl-esters to access nonsteroidal anti-inflammatory drugs (NSAIDs) on the gram scale.

Synthesis of α-Aryl nitriles through palladium-catalyzed decarboxylative coupling of cyanoacetate salts with aryl halides and triflates

Shang, Rui,Ji, Dong-Sheng,Chu, Ling,Fu, Yao,Liu, Lei

supporting information; experimental part, p. 4470 - 4474 (2011/06/24)

Worth its salt: The palladium-catalyzed decarboxylative coupling of the cyanoacetate salt as well as its mono- and disubstituted derivatives with aryl chlorides, bromides, and triflates is described (see scheme). This reaction is potentially useful for the preparation of a diverse array of α-aryl nitriles and has good functional group tolerance. S-Phos=2-(2,6- dimethoxybiphenyl)dicyclohexylphosphine), Xant-Phos=4,5-bis(diphenylphosphino)- 9,9-dimethylxanthene. Copyright

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