1072346-26-9 Usage
Description
1,10-Phenanthroline, 2,9-bis[4-(1-Methyl-1H-benziMidazol-2-yl)phenyl]-4,7-diphenylis a complex organic compound that consists of a 1,10-phenanthroline core with two 4-(1-Methyl-1H-benziMidazol-2-yl)phenyl groups attached. 1,10-Phenanthroline, 2,9-bis[4-(1-Methyl-1H-benziMidazol-2-yl)phenyl]-4,7-diphenylis characterized by its ability to chelate with metal ions, making it a valuable asset in coordination chemistry. Its unique structure also endows it with biologically active properties, which are currently being explored for potential applications in the development of new drugs. Furthermore, it has found utility in the realm of fluorescent sensors and diagnostic assays due to its selective metal ion binding capabilities.
Uses
Used in Coordination Chemistry:
1,10-Phenanthroline, 2,9-bis[4-(1-Methyl-1H-benziMidazol-2-yl)phenyl]-4,7-diphenylis used as a chelating agent for forming stable complexes with various metal ions. Its application in this field is crucial for understanding the properties and reactivity of metal complexes, which can have significant implications in areas such as catalysis and materials science.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1,10-Phenanthroline, 2,9-bis[4-(1-Methyl-1H-benziMidazol-2-yl)phenyl]-4,7-diphenylis being investigated for its potential applications in the development of new drugs. Its biologically active properties make it a promising candidate for further research and development, with the aim of creating novel therapeutic agents.
Used in Fluorescent Sensors and Diagnostic Assays:
1,10-Phenanthroline, 2,9-bis[4-(1-Methyl-1H-benziMidazol-2-yl)phenyl]-4,7-diphenylhas been utilized in the development of fluorescent sensors and diagnostic assays. Its ability to selectively bind to certain metal ions makes it a valuable tool for detecting and measuring the presence of these ions in various samples, which can be crucial in a range of applications, from environmental monitoring to medical diagnostics.
Used in Analytical Chemistry:
In analytical chemistry, 1,10-Phenanthroline, 2,9-bis[4-(1-Methyl-1H-benziMidazol-2-yl)phenyl]-4,7-diphenylcan be employed as a reagent for the detection and quantification of metal ions. Its selective binding properties allow for the development of sensitive and specific analytical methods, which can be applied in various industries, including environmental science, pharmaceuticals, and materials research.
Used in Environmental Science:
1,10-Phenanthroline, 2,9-bis[4-(1-Methyl-1H-benziMidazol-2-yl)phenyl]-4,7-diphenylis used as a detection agent for monitoring metal ion contamination in environmental samples. Its application in this field helps to ensure the safety and quality of natural resources, as well as to develop strategies for pollution control and remediation.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,10-Phenanthroline, 2,9-bis[4-(1-Methyl-1H-benziMidazol-2-yl)phenyl]-4,7-diphenylis used as a starting material or intermediate in the synthesis of various drug candidates. Its unique chemical properties and potential biological activities make it a valuable asset in the development of new therapeutic agents to treat a wide range of diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 1072346-26-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,2,3,4 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1072346-26:
(9*1)+(8*0)+(7*7)+(6*2)+(5*3)+(4*4)+(3*6)+(2*2)+(1*6)=129
129 % 10 = 9
So 1072346-26-9 is a valid CAS Registry Number.
1072346-26-9Relevant articles and documents
PHENANTHROLINE COMPOUND AND ORGANIC LIGHT EMITTING DEVICE USING THE SAME
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Page/Page column 7, (2008/12/04)
The present invention discloses a phenanthroline compound which can be used as electron-transporting material in organic electroluminescence devices is disclosed. The mentioned phenanthroline compound is represented by the following. wherein Ar is selected from the group consisting of hydrogen atom, alkyl, aryl, wherein R1, R2 and R3 are identical or different. R1, R2 and R3 are independently selected from the group consisting of hydrogen atom, alkyl, halide, wherein X1, X2 and X3 are identical or different. X1, X2 and X3 are independently selected from the atom or group consisting of O, S, N—R4 and R4 is selected from the group consisting of hydrogen atom, alkyl, aryl.
