14806-50-9 Usage
Uses
Used in Research and Diagnostic Applications:
3,3'-DIETHYLOXADICARBOCYANINE IODIDE is used as a sensitive probe for various research and diagnostic applications. Its high sensitivity makes it an ideal candidate for detecting and monitoring specific biological processes or interactions at the cellular or molecular level.
Used in Biomedical Imaging:
In the field of biomedical imaging, 3,3'-DIETHYLOXADICARBOCYANINE IODIDE is used as a fluorescent marker to visualize and track cellular structures, functions, or the behavior of specific biomolecules within living organisms. Its unique optical properties allow for the differentiation and identification of various biological components.
Used in Analytical Chemistry:
3,3'-DIETHYLOXADICARBOCYANINE IODIDE is employed as an analytical tool in various chemical assays and techniques, such as fluorescence spectroscopy and flow cytometry. Its sensitivity and specificity enable the detection and quantification of target molecules or ions in complex samples, contributing to the advancement of chemical analysis and environmental monitoring.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 3,3'-DIETHYLOXADICARBOCYANINE IODIDE is utilized as a probe to study drug interactions, binding affinities, and the mechanisms of action of potential therapeutic agents. Its sensitivity allows for the identification of novel drug targets and the optimization of drug candidates for improved efficacy and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 14806-50-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,8,0 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14806-50:
(7*1)+(6*4)+(5*8)+(4*0)+(3*6)+(2*5)+(1*0)=99
99 % 10 = 9
So 14806-50-9 is a valid CAS Registry Number.
InChI:InChI=1/C23H23N2O2.HI/c1-3-24-18-12-8-10-14-20(18)26-22(24)16-6-5-7-17-23-25(4-2)19-13-9-11-15-21(19)27-23;/h5-17H,3-4H2,1-2H3;1H/q+1;/p-1
14806-50-9Relevant academic research and scientific papers
Kim, Jong Chul,Ohga, Yasushi,Asano, Tsutomu,Weinberg, Noham N.,George, Adrian V.
, p. 103 - 111 (2001)
Pressure and viscosity effects on the rate of thermal Z/E isomerization of two carbocyanine dyes, 3,3′-diethyloxacarbocyanine iodide (DOCI) and 3,3′-diethyloxadicarbocyanine iodide, (DODCI) were measured in 2-methylpentane-2,4-diol. From the results, the following conclusions are obtained. 1. The medium and the chemical coordinates have to be treated separately, as in the reactions of uncharged species. 2. A positive charge on the reactant seems to induce an earlier deviation from the transition state theory. 3. The most important factors controlling a deviation from the transition state theory are the anisotropy of the characteristic times of reaction and solvent fluctuations, and the strength of the solute-solvent interactions.
The first unequivocal observation of dynamic solvent effects in the thermal geometrical isomerization of 3,3′-diethyloxadicarbocyanine iodide (DODCI)
Kim, Jong Chul,Ohga, Yasushi,Asano, Tsutomu
, p. 301 - 302 (2007/10/03)
Pressure dependence of the rate of thermal geometrical isomerization of 3,3′-diethyloxadicarbocyanine iodide (DODCI) was studied in ethanol and in a highly viscous hydroxylic solvent, 2-methyl-2,4-pentanediol. The kinetic effects of pressure in the two solvents are qualitatively different and the results strongly suggest that the stochastic analysis of the kinetic results in 1-alkanols reported earlier needs to be renounced.
