31354-66-2 Usage
Description
1-(2-cyanoethyl)-2-[4-(diethylamino)phenyl]benz[cd]indolium chloride is an organic compound characterized by its benz[cd]indolium core. It is cationic in nature and is known for its stability, resistance to photobleaching, and ability to bind to DNA and RNA. The presence of a cyanoethyl group in the molecule enables effective conjugation to biomolecules, making it a versatile tool in various biological labeling and detection assays.
Uses
Used in Biological and Analytical Applications:
1-(2-cyanoethyl)-2-[4-(diethylamino)phenyl]benz[cd]indolium chloride is used as a fluorescent dye for its ability to bind to DNA and RNA. Its cationic nature, stability, and resistance to photobleaching make it an ideal choice for long-term imaging studies and various biological labeling and detection assays.
Used in Research and Diagnostics:
In the field of research and diagnostics, 1-(2-cyanoethyl)-2-[4-(diethylamino)phenyl]benz[cd]indolium chloride is used as a molecular probe to study the structure, function, and interactions of nucleic acids such as DNA and RNA. Its fluorescence properties allow for the visualization and tracking of these biomolecules within cells and tissues, contributing to a better understanding of their roles in cellular processes and disease mechanisms.
Used in Drug Delivery Systems:
1-(2-cyanoethyl)-2-[4-(diethylamino)phenyl]benz[cd]indolium chloride's ability to bind to DNA and RNA, along with its cationic nature, makes it a potential candidate for use in drug delivery systems. 1-(2-cyanoethyl)-2-[4-(diethylamino)phenyl]benz[cd]indolium chloride can be employed as a carrier for the targeted delivery of therapeutic agents, such as small molecules or siRNA, to specific cells or tissues. This application can improve the efficacy and specificity of treatments, reducing side effects and enhancing patient outcomes.
Used in the Pharmaceutical Industry:
In the pharmaceutical industry, 1-(2-cyanoethyl)-2-[4-(diethylamino)phenyl]benz[cd]indolium chloride may be utilized in the development of new drugs targeting nucleic acids, such as antisense oligonucleotides or gene-editing technologies. Its properties as a fluorescent dye and molecular probe can aid in the design, synthesis, and evaluation of these therapeutic agents, ultimately contributing to the advancement of novel treatments for various diseases.
Used in the Development of Biosensors:
1-(2-cyanoethyl)-2-[4-(diethylamino)phenyl]benz[cd]indolium chloride's ability to bind to DNA and RNA, as well as its fluorescence properties, makes it a suitable candidate for the development of biosensors. 1-(2-cyanoethyl)-2-[4-(diethylamino)phenyl]benz[cd]indolium chloride can be used to create sensors that detect specific nucleic acid sequences or changes in their structure, which can be applied in environmental monitoring, food safety, and medical diagnostics.
Check Digit Verification of cas no
The CAS Registry Mumber 31354-66-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,3,5 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 31354-66:
(7*3)+(6*1)+(5*3)+(4*5)+(3*4)+(2*6)+(1*6)=92
92 % 10 = 2
So 31354-66-2 is a valid CAS Registry Number.
InChI:InChI=1/C24H24N3.ClH/c1-3-26(4-2)20-14-12-19(13-15-20)24-21-10-5-8-18-9-6-11-22(23(18)21)27(24)17-7-16-25;/h5-6,8-15H,3-4,7,17H2,1-2H3;1H/q+1;/p-1
