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2-benzo[f]quinolin-3-yl-1H-indene-1,3(2H)-dione is a unique chemical compound that falls under the category of organic compounds known as quinoline and derivatives. 2-benzo[f]quinolin-3-yl-1H-indene-1,3(2H)-dione is characterized by the presence of a quinoline moiety, which is formed by the fusion of a benzene ring with a pyridine ring. The molecular structure of 2-benzo[f]quinolin-3-yl-1H-indene-1,3(2H)-dione is intricate, featuring multiple carbon atom rings, including both quinoline and indene groups. As a specialized scientific compound, its potential applications and uses are diverse and may be subject to ongoing research to further understand its properties and possible applications. However, detailed information regarding its source, utilization, and its potential impact on human health or the environment is currently limited and would require expert scientific knowledge for precise interpretation.

63216-89-7

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63216-89-7 Usage

Uses

Used in Pharmaceutical Research:
2-benzo[f]quinolin-3-yl-1H-indene-1,3(2H)-dione is utilized as a research compound for exploring its potential pharmaceutical applications. Its complex molecular structure and the presence of quinoline and indene groups make it a candidate for investigation in drug discovery, particularly in the development of new therapeutic agents.
Used in Chemical Synthesis:
In the field of organic chemistry, 2-benzo[f]quinolin-3-yl-1H-indene-1,3(2H)-dione serves as a key intermediate in the synthesis of more complex molecules. Its unique structure allows for further chemical reactions and modifications, which can lead to the creation of novel compounds with specific properties and applications.
Used in Material Science:
2-benzo[f]quinolin-3-yl-1H-indene-1,3(2H)-dione may also find applications in material science, where its structural characteristics could be leveraged to develop new materials with tailored properties. This could include uses in the development of advanced materials for electronics, optics, or other high-tech applications.
Note: The specific applications mentioned above are hypothetical and are based on the general properties of compounds within the quinoline and derivatives class. Actual uses may vary and would depend on the results of further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 63216-89-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,2,1 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63216-89:
(7*6)+(6*3)+(5*2)+(4*1)+(3*6)+(2*8)+(1*9)=117
117 % 10 = 7
So 63216-89-7 is a valid CAS Registry Number.
InChI:InChI=1/C22H13NO2/c24-21-16-7-3-4-8-17(16)22(25)20(21)19-12-10-15-14-6-2-1-5-13(14)9-11-18(15)23-19/h1-12,20H

63216-89-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-Benzo[f]quinolyl)-1H-indene-1,3(2H)-dione

1.2 Other means of identification

Product number -
Other names 2-benzo[f]quinolin-3-yl-1H-indene-1,3(2H)-dione

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 -
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More Details:63216-89-7 SDS

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