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  • Acenaphtho[1,2-b]quinoline,10-methoxy- CAS NO.132297-89-3 CAS NO.132297-89-3

    Cas No: 132297-89-3

  • USD $ 7.0-8.0 / Metric Ton

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132297-89-3 Usage


10-methoxyacenaphtho[1,2-b]quinoline is a chemical compound characterized by a fused tricyclic structure, derived from acenaphthoquinoline, a polycyclic aromatic hydrocarbon. The distinctive addition of a methoxy group at the 10th position endows it with unique properties, making it a promising candidate for various applications due to its potential biological activity and utility as a fluorescent probe or in the development of new materials with specific properties. Its intriguing chemical structure and properties have garnered interest for further research and potential uses in diverse fields, including medicine, materials science, and organic chemistry.


Used in Pharmaceutical and Medicinal Chemistry:
10-methoxyacenaphtho[1,2-b]quinoline serves as a key intermediate in the synthesis of various pharmaceutical compounds, leveraging its unique structure to enhance drug properties such as solubility, stability, and bioavailability. Its potential biological activity makes it a valuable component in the development of new therapeutic agents.
Used as a Fluorescent Probe in Research:
In the field of scientific research, 10-methoxyacenaphtho[1,2-b]quinoline is utilized as a fluorescent probe, capitalizing on its optical properties to track and visualize molecular interactions, cellular processes, and other biological phenomena. Its fluorescence characteristics allow for sensitive detection and imaging in various experimental setups.
Used in Materials Science for Property Enhancement:
10-methoxyacenaphtho[1,2-b]quinoline is employed in materials science to confer specific properties to new materials, such as improved conductivity, stability, or photophysical behavior. Its incorporation into polymers, composites, or other material systems can lead to the development of advanced materials with tailored characteristics for specialized applications.
Used in Organic Chemistry for Synthesis:
In organic chemistry, 10-methoxyacenaphtho[1,2-b]quinoline is used as a building block or reactant in the synthesis of complex organic molecules. Its tricyclic structure and methoxy substitution provide a versatile platform for further functionalization and the creation of novel organic compounds with diverse applications.
While the provided materials do not specify particular industries or applications, the above uses are inferred based on the compound's properties and potential areas of interest. Further research and development would be necessary to explore and validate specific applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 132297-89-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,2,9 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 132297-89:
133 % 10 = 3
So 132297-89-3 is a valid CAS Registry Number.



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


1.1 GHS Product identifier

Product name 10-methoxyacenaphthyleno[2,1-b]quinoline

1.2 Other means of identification

Product number -
Other names Acenaphtho[1,2-b]quinoline,10-methoxy

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:132297-89-3 SDS

132297-89-3Downstream Products

132297-89-3Relevant articles and documents

Studies on Polycyclic Azaarenes. 3. Stereoselective Synthesis of trans-10,11-Dihydroxy-10,11-dihydrodibenzacridine and trans-10,11-Dihydroxy-10,11-dihydroacenaphthoquinoline

Ray, Jayanta K.,Kar, Gandhi K.,Karmakar, Arun C.

, p. 2268 - 2270 (2007/10/02)


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