586409-05-4 Usage
Uses
Used in Pharmaceutical Synthesis:
6-Methylthiazolo[4,5-b]pyridine-2-thiol serves as a key intermediate in the synthesis of pharmaceuticals, contributing to the development of novel drugs with potential therapeutic applications. Its unique structure allows for the creation of compounds with specific biological activities, making it valuable in medicinal chemistry.
Used in Agrochemical Production:
In the agrochemical industry, 6-Methylthiazolo[4,5-b]pyridine-2-thiol is utilized in the production of pesticides and other crop protection agents. Its chemical properties enable the design of effective compounds that can protect crops from pests and diseases, thereby enhancing agricultural productivity.
Used in Material Science:
6-Methylthiazolo[4,5-b]pyridine-2-thiol also finds applications in material science, where its distinctive structure and properties can be harnessed to develop new materials with unique characteristics. This includes potential uses in the creation of advanced polymers, sensors, or other innovative materials with specific applications.
Overall, the diverse applications of 6-Methylthiazolo[4,5-b]pyridine-2-thiol underscore its versatility and the broad impact it can have across different industries, from healthcare to agriculture and beyond.
Check Digit Verification of cas no
The CAS Registry Mumber 586409-05-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,6,4,0 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 586409-05:
(8*5)+(7*8)+(6*6)+(5*4)+(4*0)+(3*9)+(2*0)+(1*5)=184
184 % 10 = 4
So 586409-05-4 is a valid CAS Registry Number.
586409-05-4Relevant academic research and scientific papers
Synthesis and study of nucleic acids interactions of novel monomethine cyanine dyes
Kaloyanova, Stefka,Crnolatac, Ivo,Lesev, Nedyalko,Piantanida, Ivo,Deligeorgiev, Todor
scheme or table, p. 1184 - 1191 (2012/03/27)
Six asymmetric monomethine cyanine dyes have been synthesized and their spectral characteristics and interaction with double stranded (ds)DNA have been investigated for their prospective use as fluorescent markers in molecular biology. Therefore, the non-covalent binding of the compounds with dsDNA was explored. Apart from the fluorescence spectroscopy, the study includes UV/Vis spectrophotometry and circular dichroism spectroscopy, as well as the thermal melting experiments. Although the compounds show relatively low binding affinity toward dsDNA and do not have intrinsic fluorescence, in the presence of dsDNA they exhibited considerable enhancement in fluorescence intensity. Therefore the studied dyes show interesting platform for future modifications directed toward more sequence selective derivatives. The compound with the highest affinity toward dsDNA showed interesting anti-proliferative potential and specificity.
