7243-06-3 Usage
Uses
Used in Organic Synthesis:
2,3,4,5,6-PENTAFLUOROPHENYL 5-(DIMETHYLAMINO)-1-NAPHTHALENESULFONATE is used as a reagent in organic synthesis for the creation of various chemical compounds, leveraging its unique chemical properties to facilitate reactions and form desired products.
Used in Fluorescent Labeling:
In the field of molecular biology, 2,3,4,5,6-PENTAFLUOROPHENYL 5-(DIMETHYLAMINO)-1-NAPHTHALENESULFONATE is used as a fluorescent labeling agent for amino acids in peptide synthesis. Its strong fluorescence allows for the tracking and detection of specific molecules within complex biological systems.
Used in Pharmaceutical Research:
2,3,4,5,6-PENTAFLUOROPHENYL 5-(DIMETHYLAMINO)-1-NAPHTHALENESULFONATE is employed in pharmaceutical research as a fluorescent probe for the investigation of biological systems. Its ability to label and image proteins aids in the study of their structure, function, and interactions within the body.
Used in the Study of Protein-Protein Interactions:
In the field of biochemistry, 2,3,4,5,6-PENTAFLUOROPHENYL 5-(DIMETHYLAMINO)-1-NAPHTHALENESULFONATE is used as a tool to study protein-protein interactions. Its fluorescent properties allow researchers to observe and analyze how proteins interact with each other, which is crucial for understanding various biological processes and diseases.
Used in the Study of Protein Folding:
2,3,4,5,6-PENTAFLUOROPHENYL 5-(DIMETHYLAMINO)-1-NAPHTHALENESULFONATE is also used in the study of protein folding, a critical process in which proteins assume their functional three-dimensional structures. 2,3,4,5,6-PENTAFLUOROPHENYL 5-(DIMETHYLAMINO)-1-NAPHTHALENESULFONATE's fluorescent properties help researchers monitor the folding process and identify misfolded proteins, which are associated with several diseases.
Used in Imaging Biological Systems:
In the broader field of bioimaging, 2,3,4,5,6-PENTAFLUOROPHENYL 5-(DIMETHYLAMINO)-1-NAPHTHALENESULFONATE is used as a fluorescent probe to visualize and study the structure and dynamics of biological systems at the molecular level. This aids in advancing our understanding of cellular processes and the development of new therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 7243-06-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,4 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7243-06:
(6*7)+(5*2)+(4*4)+(3*3)+(2*0)+(1*6)=83
83 % 10 = 3
So 7243-06-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H12F5NO3S/c1-24(2)11-7-3-6-10-9(11)5-4-8-12(10)28(25,26)27-18-16(22)14(20)13(19)15(21)17(18)23/h3-8H,1-2H3
