200862-70-0 Usage
Uses
Used in Time-Resolved Fluoroimmunoassay:
4,4''-BIS(4,4,5,5,6,6,6-HEPTAFLUORO-1,3-DIOXOHEXYL)-O-TERPHENYL-4'-SULFONYL CHLO functions as a sensitive label in time-resolved fluoroimmunoassay (TRFIA) via the europium chelate. Its large Stoke's shift and optical characteristics contribute to the enhanced sensitivity and accuracy of TRFIA tests.
Used in the Preparation of Silica-Nanoparticles:
In the field of nanotechnology, 4,4''-BIS(4,4,5,5,6,6,6-HEPTAFLUORO-1,3-DIOXOHEXYL)-O-TERPHENYL-4'-SULFONYL CHLO serves as a ligand for TRF-complexes with Eu3+. This role is instrumental in the preparation of silica-nanoparticles, which have potential applications in various industries, including biomedical, pharmaceutical, and material science.
Used in Analytical Chemistry:
The unique optical properties of 4,4''-BIS(4,4,5,5,6,6,6-HEPTAFLUORO-1,3-DIOXOHEXYL)-O-TERPHENYL-4'-SULFONYL CHLO make it a valuable tool in analytical chemistry. Its broad excitation and narrow emission bands allow for precise detection and measurement in complex samples, improving the efficiency and reliability of analytical processes.
Used in Pharmaceutical Research:
Due to its distinctive structure and properties, 4,4''-BIS(4,4,5,5,6,6,6-HEPTAFLUORO-1,3-DIOXOHEXYL)-O-TERPHENYL-4'-SULFONYL CHLO may be utilized in pharmaceutical research for the development of new drugs and drug delivery systems. Its potential interactions with biological molecules could lead to the discovery of novel therapeutic agents and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 200862-70-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,8,6 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 200862-70:
(8*2)+(7*0)+(6*0)+(5*8)+(4*6)+(3*2)+(2*7)+(1*0)=100
100 % 10 = 0
So 200862-70-0 is a valid CAS Registry Number.
200862-70-0Relevant articles and documents
Assay of substance in biological sample using labeled probe
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Referential example 3, (2008/06/13)
A method for analyzing an objective substance, comprsing reacting a labeled probe with an objective substance on a biological sample, said probe comprsing a label substance of the formula (I): wherein A1is an aromatic group, R1is a hydrogen or —COCH2COCnF2n+1and n is an integer of 1-6, which is bonded to a probe selected from the group consisting of nucleic acid, nudeic acid binding potein, low molecular ligand and receptor for ligand (except antibody) to give a fluorescent complex, reacting the complex with an objective substance on a biolgical sample and assaying fluorescence of the resultant fluorescent complex, a labeled nucleic acid probe and a labeled nucleotide. According to the method of the present invention, defects such as hindrance of fluorescence due to contaminant substance, low sensitivity and the like can be resolved, thereby enabling analysis on a tissue.