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Sku CI23293_25_G
Chem Impex
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Product Information

Product Name
4-Morpholinobenzoic acid
Brand Name
Chem Impex
Product Number
23293
CAS
7470-38-4
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
345278
IUPAC Name
4-morpholin-4-ylbenzoic acid
InChI Key
XVAJKPNTGSKZSQ-UHFFFAOYSA-N
SMILES
C1COCCN1C2=CC=C(C=C2)C(=O)O

Application

4-Morpholinobenzoic acid is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly in developing drugs targeting neurological disorders.

Polymer Chemistry: It acts as a building block for creating specialty polymers, enhancing material properties such as flexibility and durability in applications like coatings and adhesives.

Biochemical Research: Researchers use it as a reagent in biochemical assays, aiding in the study of enzyme activity and protein interactions, which is crucial for drug discovery.

Agricultural Chemicals: Its derivatives are explored for use in agrochemicals, contributing to the development of effective herbicides and pesticides with lower environmental impact.

Analytical Chemistry: The compound is employed in analytical methods for detecting and quantifying other substances, providing reliable results in quality control processes.

References

Discovery of small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase

Publication Name: Journal of Enzyme Inhibition and Medicinal Chemistry
Publication Date: 2022-05-05
DOI: 10.1080/14756366.2022.2070909

Classical Methodologies

Publication Name: Science of Synthesis
Publication Date: 2016

A High-Throughput Assay to Identify Inhibitors of the Apicoplast DNA Polymerase from Plasmodium falciparum

Publication Name: Journal of biomolecular screening
Publication Date: 2014-07
DOI: 10.1177/1087057114528738

High-throughput screening identification of poliovirus RNA-dependent RNA polymerase inhibitors

Publication Name: Antiviral Research
Publication Date: 2011-09
DOI: 10.1016/j.antiviral.2011.06.006