824401-53-8 Usage
Chemical structure
A complex compound with a macrocyclic structure containing four nitrogen atoms and three molecules of 4-(1,1-dimethylethyl)phenylmethyl attached through ester linkages.
Functional groups
Contains ester groups and 1,1-dimethylethyl ester groups.
Applications
Potential uses in coordination chemistry, as a chelating agent, and in medicinal chemistry for targeted drug delivery.
Unique properties
The complex nature of the compound suggests it may have unique properties and potential uses in various fields of science and technology.
Derivative
It is a derivative of 1,4,7,10-tetraazacyclododecane, a macrocyclic compound with four nitrogen atoms.
Molecular weight
Approximately 708.11 g/mol
Solubility
The solubility of 1,4,7,10-Tetraazacyclododecane-1-acetic acid,
4,7,10-tris[[4-(1,1-dimethylethyl)phenyl]methyl]-, 1,1-dimethylethyl ester is not explicitly mentioned in the provided material, but it is likely soluble in organic solvents due to its ester and non-polar groups.
Stability
The stability of 1,4,7,10-Tetraazacyclododecane-1-acetic acid,
4,7,10-tris[[4-(1,1-dimethylethyl)phenyl]methyl]-, 1,1-dimethylethyl ester is not explicitly mentioned in the provided material, but it is expected to be stable under normal conditions due to the presence of strong covalent bonds within the molecule.
Check Digit Verification of cas no
The CAS Registry Mumber 824401-53-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,4,4,0 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 824401-53:
(8*8)+(7*2)+(6*4)+(5*4)+(4*0)+(3*1)+(2*5)+(1*3)=138
138 % 10 = 8
So 824401-53-8 is a valid CAS Registry Number.
824401-53-8Relevant academic research and scientific papers
Comparative in vivo behavior studies of cyclen-based copper-64 complexes: Regioselective synthesis, X-ray structure, radiochemistry, log P, and biodistribution
Yoo, Jeongsoo,Reichert, David E.,Welch, Michael J.
, p. 6625 - 6637 (2007/10/03)
The in vivo behavior of copper(II)-cyclen complexes was modified via substitution of the parent ligand with two different substituents, 4-tert-butylbenzyl and acetate. This was achieved by using same synthetic strategy (regioselective protection/first alk
Regioselective N-substitution of cyclen with two different alkyl groups: Synthesis of all possible isomers
Yoo, Jeongsoo,Reichert, David E.,Welch, Michael J.
, p. 766 - 767 (2007/10/03)
All possible configurations of two different groups on the four nitrogen atoms of cyclen were achieved using four differently protected cyclen intermediates including the novel mono-protected cyclen compound, mono-N-Cbz-cyclen.
