1244034-02-3 Usage
Uses
Used in Research and Diagnostic Applications:
SULFORHODAMINEAMIDOETHYL MERCAPTAN is used as a fluorescent probe for various research and diagnostic applications due to its distinct absorption and emission spectra. Its deep red color and fluorescence properties make it suitable for detecting and monitoring biological processes and interactions.
Used in Analytical Chemistry:
In the field of analytical chemistry, SULFORHODAMINEAMIDOETHYL MERCAPTAN is used as a reagent for the detection and quantification of specific molecules or ions. Its fluorescent properties allow for sensitive and selective detection in various analytical techniques.
Used in Biomedical Applications:
SULFORHODAMINEAMIDOETHYL MERCAPTAN is employed as a contrast agent in biomedical imaging, such as fluorescence microscopy and other imaging modalities. Its ability to emit fluorescence upon excitation makes it a valuable tool for visualizing cellular structures and processes in living organisms.
Used in Pharmaceutical Development:
In the pharmaceutical industry, SULFORHODAMINEAMIDOETHYL MERCAPTAN is used as a starting material or intermediate in the synthesis of various drugs and drug candidates. Its unique chemical properties can be exploited to develop new therapeutic agents with potential applications in treating various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 1244034-02-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,4,0,3 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1244034-02:
(9*1)+(8*2)+(7*4)+(6*4)+(5*0)+(4*3)+(3*4)+(2*0)+(1*2)=103
103 % 10 = 3
So 1244034-02-3 is a valid CAS Registry Number.
1244034-02-3Relevant academic research and scientific papers
Click chemistry by microcontact printing on self-assembled monolayers: A structure-reactivity study by fluorescence microscopy
Mehlich, Jan,Ravoo, Bart Jan
, p. 4108 - 4115 (2011/07/07)
Microcontact printing (μCP) has developed into a powerful tool to functionalize surfaces with patterned molecular monolayers. μCP can also be used to induce a chemical reaction between a molecular ink and a self-assembled monolayer (SAM) in the nanoscale confinement between stamp and substrate. In this paper, we investigate the Huisgen 1,3-dipolar cycloaddition, the Diels-Alder cycloaddition and the thiol-ene/yne reaction induced by μCP. A range of fluorescent alkyne inks were printed on azide SAMs and fluorescence microscopy was used to monitor the extent of the 1,3-dipolar cycloaddition on a glass substrate. The rate of cycloaddition depends on the reactivity of the alkyne and on the presence of Cu(i). The cycloaddition is accelerated by Cu(i) but it also proceeds readily in the absence of Cu(i). In addition, a range of fluorescent diene inks were printed on alkene SAMs on glass. In this case, fluorescence microscopy was used to monitor the rate of the Diels-Alder cycloaddition as well as its retro-reaction. Finally, fluorescent thiol inks were printed on alkene SAMs on glass, and fluorescent alkenes and alkynes were printed on thiol SAMs. It is shown that reactions by μCP follow structure-reactivity relationships similar to solution reactions. Under optimized conditions all reactions lead to dense microarrays of addition products within minutes of printing time.
