37067-12-2 Usage
Description
Methyl 1,10-phenanthroline-2-carboxylate is a chemical compound with a molecular formula C15H11N2O2. It is a derivative of phenanthroline, a heterocyclic compound widely used in coordination chemistry and as a ligand in metal complexes. This versatile chemical possesses diverse potential applications in various scientific and industrial fields, including catalysis, fluorescence labeling, and as a building block in the synthesis of organic compounds. Additionally, it may have uses in biological and pharmaceutical research, although further studies are required to fully explore its potential in these areas.
Uses
Used in Catalysis:
Methyl 1,10-phenanthroline-2-carboxylate is used as a catalyst in various chemical reactions due to its ability to form stable metal complexes. Its coordination with metal ions enhances the catalytic activity and selectivity of the reactions, making it a valuable component in the development of efficient and environmentally friendly catalytic processes.
Used in Fluorescence Labeling:
In the field of molecular biology and biochemistry, Methyl 1,10-phenanthroline-2-carboxylate is used as a fluorescence labeling agent. Its fluorescent properties allow for the tracking and visualization of biomolecules, such as proteins and nucleic acids, in various experimental setups. This application aids researchers in gaining insights into the structure, function, and interactions of these biomolecules.
Used in Organic Synthesis:
Methyl 1,10-phenanthroline-2-carboxylate serves as a building block in the synthesis of various organic compounds. Its unique structure and reactivity make it a useful component in the creation of complex organic molecules, which can be applied in pharmaceuticals, materials science, and other related fields.
Used in Biological and Pharmaceutical Research:
Although further studies are needed, Methyl 1,10-phenanthroline-2-carboxylate may have potential applications in biological and pharmaceutical research. Its ability to form metal complexes and interact with biomolecules could lead to the development of new drugs, diagnostic tools, or therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 37067-12-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,0,6 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 37067-12:
(7*3)+(6*7)+(5*0)+(4*6)+(3*7)+(2*1)+(1*2)=112
112 % 10 = 2
So 37067-12-2 is a valid CAS Registry Number.
37067-12-2Relevant articles and documents
Substituted phenanthrolines as antennae in luminescent EuIII complexes
Akerboom, Sebastiaan,Van Den Elshout, Jos J. M. H.,Mutikainen, Ilpo,Siegler, Maxime A.,Fu, Wen Tian,Bouwman, Elisabeth
supporting information, p. 6137 - 6146 (2014/01/06)
Eight novel europium(III)-based coordination compounds with 1,10-phenanthroline (phen) ligands with a chloro, methoxy, ethoxy, cyano, carboxylic acid, methyl carboxylate, ethyl carboxylate, and amino substituent on the 2-position have been prepared in yields ranging from 43 to 89 %. Additionally, one lanthanum(III) coordination compound of 2-amino-1,10- phenanthroline has been isolated. All compounds have the general formula [Ln(L)2(NO3)3], except for the compound with the carboxylate ligand, which has the formula [Eu(O2Cphen) 3]. Three of the EuIII complexes as well as the La III compound crystal structures have been determined, all of which show similar N4O6 coordination spheres for the Ln III ion. Seven compounds exhibit bright luminescence that is characteristic of EuIII upon irradiation with near-UV radiation, thus indicating efficient ligand-to-metal energy transfer. The complex with 2-amino-1,10-phenanthroline is nonluminescent. The solid-state photoluminescent quantum yields range from 10 to 79 %, and the luminescence lifetimes vary from 0.43 to 1.57 ms. Analysis of the spectral intensities with the Judd-Ofelt theory shows a significant contribution of nonradiative processes that quench the luminescence of the 5D0 level on EuIII. Eight new EuIII complexes with 1,10-phenanthroline ligands substituted on the 2-position have been prepared, analyzed, and the photoluminescence properties studied. The complex with the 2-chloro substituent exhibits bright photoluminescence with a high quantum yield of 78 %. The complex with the 2-amino substituent is nonluminescent. Copyright
Carboxylic and Phosphate Ester Hydrolysis Catalysed by Bivalent Zinc and Coper Metallosurfactants
Weijnen, John G. F.,Koudijs, Arie,Engbersen, Johan F. J.
, p. 1121 - 1126 (2007/10/02)
The synthesis of three new lipophilic ligands are reported: Nα-(1,10-phenanthrolin-2-ylmethyl)-N-τ-dodecylhistamine (1), N-dodecyl-2-aminomethyl-1,10-phenanthroline (2), and Nα-(2-pyridylmethyl)-Nτ-dodecylhistam
