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2-NAPHTHALEN-2-YL-QUINOLINE-4-CARBOXYLIC ACID is a chemical compound with a molecular formula C19H13NO2, derived from the fusion of quinoline and naphthalene, two aromatic hydrocarbons. 2-NAPHTHALEN-2-YL-QUINOLINE-4-CARBOXYLIC ACID features a quinoline ring system with a carboxylic acid group at the 4-carbon position and a naphthalene group at the 2-carbon position. It is recognized for its potential biological activities and is primarily utilized in the field of medicinal chemistry.

13605-87-3

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13605-87-3 Usage

Uses

Used in Medicinal Chemistry:
2-NAPHTHALEN-2-YL-QUINOLINE-4-CARBOXYLIC ACID is used as a pharmaceutical candidate for its demonstrated anti-inflammatory, antimicrobial, and antitumor properties. Its ability to modulate biochemical pathways involved in various diseases makes it a promising agent for the development of new therapeutics.
Used in Anti-Inflammatory Applications:
In the field of anti-inflammatory research, 2-NAPHTHALEN-2-YL-QUINOLINE-4-CARBOXYLIC ACID is used as an agent to potentially reduce inflammation, offering a new avenue for treating conditions characterized by excessive inflammatory responses.
Used in Antimicrobial Applications:
2-NAPHTHALEN-2-YL-QUINOLINE-4-CARBOXYLIC ACID is utilized as an antimicrobial agent, targeting a range of microorganisms and contributing to the development of new antibiotics to combat drug-resistant infections.
Used in Antitumor Applications:
In oncology, 2-NAPHTHALEN-2-YL-QUINOLINE-4-CARBOXYLIC ACID is employed as an antitumor agent, with studies indicating its potential to inhibit the growth and spread of cancer cells, making it a candidate for further research in cancer treatment.
Used in Biochemical Pathway Inhibition:
2-NAPHTHALEN-2-YL-QUINOLINE-4-CARBOXYLIC ACID is used as an inhibitor of specific biochemical pathways, which may play a role in the pathogenesis of certain diseases, thus offering a strategy for disease intervention and management.
Further research on 2-NAPHTHALEN-2-YL-QUINOLINE-4-CARBOXYLIC ACID is ongoing to explore its potential applications in various therapeutic areas, highlighting its versatility and significance in the realm of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 13605-87-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,0 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13605-87:
(7*1)+(6*3)+(5*6)+(4*0)+(3*5)+(2*8)+(1*7)=93
93 % 10 = 3
So 13605-87-3 is a valid CAS Registry Number.

13605-87-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-naphthalen-2-ylquinoline-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-[2]Naphthyl-chinolin-4-carbonsaeure

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:13605-87-3 SDS

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