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2-Ethyl-3-methyl-quinoline-4-carboxylic acid is a quinoline carboxylic acid derivative with the molecular formula C14H13NO2. It features a quinoline ring with an ethyl and a methyl group attached, along with a carboxylic acid functional group. This chemical compound is of interest in the pharmaceutical industry due to its potential as a drug intermediate and has been studied for its potential biological activities, such as antimicrobial and anti-inflammatory properties. Its synthesis and potential applications in drug development make it a significant compound in medicinal chemistry research.

74960-58-0

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74960-58-0 Usage

Uses

Used in Pharmaceutical Industry:
2-Ethyl-3-methyl-quinoline-4-carboxylic acid is used as a drug intermediate for the development of new pharmaceuticals. Its unique structure and functional groups make it a promising candidate for the synthesis of various medicinal compounds.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2-Ethyl-3-methyl-quinoline-4-carboxylic acid is used for studying its potential biological activities, such as antimicrobial and anti-inflammatory properties. This research aids in understanding its therapeutic potential and contributes to the discovery of novel drugs.
Used in Drug Synthesis:
2-Ethyl-3-methyl-quinoline-4-carboxylic acid is utilized as a key component in the synthesis of various drugs. Its presence in the molecular structure can influence the pharmacological properties of the final drug product, making it an essential component in drug development processes.
Used in Antimicrobial Applications:
2-Ethyl-3-methyl-quinoline-4-carboxylic acid is studied for its potential antimicrobial properties, which can be harnessed in the development of new antibiotics or antimicrobial agents to combat resistant bacterial strains.
Used in Anti-inflammatory Applications:
2-ETHYL-3-METHYL-QUINOLINE-4-CARBOXYLIC ACID is also investigated for its anti-inflammatory properties, which can be beneficial in the treatment of various inflammatory conditions and diseases. Its potential use in this area could lead to the development of new anti-inflammatory drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 74960-58-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,9,6 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 74960-58:
(7*7)+(6*4)+(5*9)+(4*6)+(3*0)+(2*5)+(1*8)=160
160 % 10 = 0
So 74960-58-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H13NO2/c1-3-10-8(2)12(13(15)16)9-6-4-5-7-11(9)14-10/h4-7H,3H2,1-2H3,(H,15,16)/p-1

74960-58-0SDS

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 2-ethyl-3-methylquinoline-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-Ethyl-3-methyl-quinoline-4-carboxylic acid

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:74960-58-0 SDS

74960-58-0Relevant academic research and scientific papers

Microwave-assisted synthesis of quinoline derivatives from isatin

El Ashry, El Sayed H.,Ramadan, El Sayed,Hamid, Hamida Abdel,Hagar, Mohamed

, p. 2243 - 2250 (2007/10/03)

Microwave irradiation has been used for a rapid and efficient synthesis of quinoline-4-carboxylic acids 5a-g and 1,2,3,4-tetrahydroacridine-9-carboxylic acid (6) from the reaction of isatins 1-3 with acyclic and cyclic ketones in basic medium. 2-Hydroxyquinoline-4-carboxylic acid (11) was also obtained by irradiating a mixture of isatin 1 and malonic acid in AcOH. The esters of 5f and 11 and their respective hydrazides 8 and 13 were also prepared under MWI. Copyright Taylor & Francis, Inc.

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