131124-59-9 Usage
Uses
Used in Analytical Chemistry:
3-(4-carboxybenzoyl)-2-quinolinecarboxaldehyde is used as an amine-reactive fluorescent probe for detecting and analyzing primary amines. The compound reacts with primary amines to form conjugates that can be analyzed using electrophoretic or chromatographic methods, providing a sensitive and selective approach to amine detection in various samples.
Used in Diagnostic Applications:
In the field of diagnostics, 3-(4-carboxybenzoyl)-2-quinolinecarboxaldehyde can be employed as a labeling agent for biomolecules, such as proteins or nucleic acids, that contain primary amine groups. The fluorescent conjugates formed can be used for various diagnostic purposes, including the detection of specific biomarkers, monitoring of biological processes, and imaging of cellular components.
Used in Research and Development:
3-(4-carboxybenzoyl)-2-quinolinecarboxaldehyde is also valuable in research and development, particularly in the fields of biochemistry, molecular biology, and drug discovery. The compound can be used to study the interactions between primary amines and other biomolecules, as well as to develop new fluorescent probes and labeling techniques for various applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-(4-carboxybenzoyl)-2-quinolinecarboxaldehyde can be utilized as a starting material or intermediate in the synthesis of novel drug candidates with potential therapeutic applications. The compound's unique structure and reactivity make it a promising candidate for the development of new drugs targeting various diseases and conditions.
Used in Material Science:
3-(4-carboxybenzoyl)-2-quinolinecarboxaldehyde can also find applications in material science, particularly in the development of new fluorescent materials and sensors. The compound's ability to form conjugates with primary amines can be exploited to create materials with tailored properties, such as enhanced sensitivity to specific analytes or improved stability under various conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 131124-59-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,1,2 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 131124-59:
(8*1)+(7*3)+(6*1)+(5*1)+(4*2)+(3*4)+(2*5)+(1*9)=79
79 % 10 = 9
So 131124-59-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H11NO4/c20-10-16-14(9-13-3-1-2-4-15(13)19-16)17(21)11-5-7-12(8-6-11)18(22)23/h1-10H,(H,22,23)
131124-59-9Relevant academic research and scientific papers
Design of 3-(4-carboxybenzoyl)-2-quinolinecarboxaldehyde as a reagent for ultrasensitive determination of primary amines by capillary electrophoresis using laser fluorescence detection
Liu, Jinping,Hsieh, You-Zoung,Wiesler, Donald,Novotny, Milos
, p. 408 - 412 (2007/10/02)
Amino acids and peptides, from both standard solutions and biological samples, were successfully reacted with 3-(4-carboxybenzoyl)-2-quinolinecarboxaldehyde, at low concentration, to form highly fluorescent isoindole derivatives. The formed mixtures are e
