57207-22-4 Usage
Uses
Used in Organic Synthesis:
(+)-(18-CROWN-6)-2,3,11,12-TETRACARBOXAMIDE is used as a synthetic reagent for facilitating various chemical reactions in the field of organic synthesis. Its crown ether structure allows it to complex with metal ions, which can be beneficial for reactions that require the presence of such ions for catalysis or stabilization of intermediates.
Used in Analytical Chemistry:
In Analytical Chemistry, (+)-(18-CROWN-6)-2,3,11,12-TETRACARBOXAMIDE is used as a chelating agent for the selective recognition and separation of metal ions. Its ability to form stable complexes with specific metal ions can be exploited in techniques such as ion-selective electrodes, chromatography, and spectroscopy for accurate detection and quantification of metal ions in various samples.
Used in Coordination Chemistry:
In Coordination Chemistry, (+)-(18-CROWN-6)-2,3,11,12-TETRACARBOXAMIDE is used as a ligand to form coordination complexes with metal ions. These complexes can exhibit unique properties, such as enhanced stability, selectivity, or reactivity, which can be harnessed for various applications, including catalysis, drug design, and materials science.
Used in Supramolecular Chemistry:
In Supramolecular Chemistry, (+)-(18-CROWN-6)-2,3,11,12-TETRACARBOXAMIDE is used as a building block for the construction of more complex molecular structures. Its ability to form host-guest complexes with metal ions can be utilized to create self-assembled systems with specific functions, such as molecular recognition, sensing, or transport.
Used in Pharmaceutical Industry:
(+)-(18-CROWN-6)-2,3,11,12-TETRACARBOXAMIDE is used as a potential therapeutic agent in the pharmaceutical industry. Its metal-ion binding properties can be exploited for the development of drugs that target metal ion-dependent biological processes, such as enzyme inhibition or modulation of ion channels.
Used in Environmental Applications:
In Environmental Applications, (+)-(18-CROWN-6)-2,3,11,12-TETRACARBOXAMIDE can be used for the selective removal of metal ions from contaminated water or soil. Its ability to form stable complexes with metal ions can help in the development of efficient and selective methods for metal ion remediation, contributing to environmental protection and sustainability.
Check Digit Verification of cas no
The CAS Registry Mumber 57207-22-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,2,0 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 57207-22:
(7*5)+(6*7)+(5*2)+(4*0)+(3*7)+(2*2)+(1*2)=114
114 % 10 = 4
So 57207-22-4 is a valid CAS Registry Number.
57207-22-4Relevant articles and documents
SYNTHESIS OF CROWN ETHERS FROM (+)-TARTARIC ACID : IMPROVED PROCEDURES
Anantanarayan, A.,Carmicheal, V.A.,Dutton, P.J.,Fyles, T.M.,Pitre, M.J.
, p. 1771 - 1776 (2007/10/02)
The synthesis of crown ethers incorporating tartaric acid units has been systematically examined.The optimum syntheses utilize oligoethylene glycol ditosylates, the bis-dimethylamide of tartaric acid, and sodium hydride as the base.The reaction conditions preserve the chiral centers.
Molecular Receptors. Functionalized and Chiral Macrocyclic Polyethers Derived from Tartaric Acid
Behr, Jean-Paul,Girodeau, Jean-Marc,Hayward, Rodney C.,Lehn, Jean-Marie,Sauvage, Jean-Pierre
, p. 2096 - 2111 (2007/10/02)
A number of functionalized and chiral macrocyclic polyethers have been synthesized by condensation of the dithallium alcoholate of (R,R)-(+)-tartaric acid derivatives with α,ω-dihalides.In this way for instance, the tetracarboxylic -O6 macrocycle 3c a
