160219-82-9 Usage
Uses
Used in Pharmaceutical Synthesis:
4-(Allylamino)-3-nitrobenzoic acid is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the development of new drugs with potential therapeutic benefits.
Used in Fluorescent Probing:
ANBA is used as a fluorescent probe for detecting cellular proteins. Its fluorescence properties enable researchers to track and visualize the distribution and interactions of proteins within cells, providing valuable insights into cellular processes and mechanisms.
Used in Receptor-Ligand Interaction Studies:
4-(Allylamino)-3-nitrobenzoic acid is used as a valuable tool in studying receptor-ligand interactions. Its ability to bind to specific receptors and exhibit fluorescence upon binding allows researchers to investigate the binding affinity, selectivity, and dynamics of these interactions, contributing to a better understanding of biological systems and the development of targeted therapies.
Used in Drug Development:
ANBA has potential applications in drug development, particularly in the discovery and optimization of new drug candidates. Its unique chemical properties and fluorescence characteristics make it a promising starting point for the design of novel therapeutic agents with improved efficacy and selectivity.
Used in Molecular Imaging:
4-(Allylamino)-3-nitrobenzoic acid is used in molecular imaging techniques, such as fluorescence microscopy and fluorescence resonance energy transfer (FRET), to visualize and study molecular processes in living cells and tissues. Its fluorescence properties enable the detection and monitoring of specific molecular events, providing valuable information for research and diagnostic applications.
Used in Analytical and Diagnostic Research:
ANBA is used in analytical and diagnostic research for its UV absorbance and fluorescence properties. It can be employed as a detection reagent or a reference standard in various analytical techniques, such as high-performance liquid chromatography (HPLC), mass spectrometry, and spectrophotometry, to improve the sensitivity and accuracy of these methods in biological and chemical analysis.
Check Digit Verification of cas no
The CAS Registry Mumber 160219-82-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,2,1 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 160219-82:
(8*1)+(7*6)+(6*0)+(5*2)+(4*1)+(3*9)+(2*8)+(1*2)=109
109 % 10 = 9
So 160219-82-9 is a valid CAS Registry Number.
