CAS 223719-29-7
:D(Me3C)CH18C6
Description:
D(Me3C)CH18C6, also known as a derivative of crown ethers, is a chemical compound characterized by its ability to selectively bind cations due to its cyclic structure. The "18C6" in its name indicates that it is a crown ether with 18 carbon atoms and 6 oxygen atoms in its ring, which provides a cavity suitable for encapsulating various metal ions, particularly alkali and alkaline earth metals. The presence of the tert-butyl group (Me3C) enhances its solubility in organic solvents and can influence its binding properties. This compound is often utilized in coordination chemistry and supramolecular chemistry for its ability to form complexes with metal ions, facilitating applications in extraction processes, ion-selective electrodes, and as a ligand in catalysis. Its unique structure allows for selective ion recognition, making it valuable in both research and industrial applications. The compound's stability, solubility, and binding characteristics are influenced by its molecular structure and the nature of the substituents attached to the crown ether framework.
Formula:C28H52O6
Synonyms:- 2,13(or 2,14)-Bis(1,1-dimethylethyl)eicosahydrodibenzo[b,k][1,4,7,10,13,16]hexaoxacyclooctadecin
- 4,4'(5')-Bis(tert-butylcyclohexano)-18-crown-6
- 4,4'(5')-[Di-tert-butyldicyclohexano]-18-crown-6
- 4,4',(5')-Di(T-Butyldicyclohexano)-18-Crown-6
- 4,4′(5′)-Di-t-butylcyclohexano-18-crown-6
- 4,4′,(5′)-Di-(tert-butylcyclohexano)-18-crown-6
- D(Me3C)CH18C6
- D(Me<sub>3</sub>C)CH18C6
- DtBuCH<sub>18</sub>C<sub>6</sub>
- Dibenzo[b,k][1,4,7,10,13,16]hexaoxacyclooctadecin, 2,13(or 2,14)-bis(1,1-dimethylethyl)eicosahydro-
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Found 3 products.
4,4',(5')-Di(t-butyldicyclohexano)-18-crown-6
CAS:4,4',(5')-Di(t-butyldicyclohexano)-18-crown-6Purity:97%Molecular weight:969.44g/mol4′,4″(5″)-Di-tert-butyldicyclohexano-18-crown-6
CAS:4',4''(5'')-Di-tert-butyldicyclohexano-18-crown-7 is a diluent and solvent that is used to dissolve other substances. It is a white, crystalline powder that has a high melting point, low vapor pressure, and low solubility in water. This product is not soluble in acid solutions, which makes it useful as a diluent for death (e.g., trichloroacetic) or acidic compounds that are damaging to living cells or tissue. 4',4''(5'')-Di-tert-butyldicyclohexano-18-crown-7 has been shown to be effective at inhibiting the growth of bacteria by preventing cell cycle phase progression and interfering with ionophores and bacterial membrane function. It also has properties that make it an excellent solvent for chloride ions in high salt environments, such as deionized water containing high concentrations ofFormula:C28H52O6Purity:Min. 95%Molecular weight:484.71 g/mol4,4’,(5’)-Di-(tert-butylcyclohexano)-18-crown-6
CAS:Controlled Product<p>Applications 4,4’,(5’)-Di-(tert-butylcyclohexano)-18-crown-6 is a crown ether-based sorbent used in the analysis and separation of minerals.<br>References Yankovskaya, V. et al: J. Radioanal. Nucl. Chem., 314, 119 (2017);<br></p>Formula:C28H52O6Color and Shape:NeatMolecular weight:500.751


