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226420-39-9

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226420-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 226420-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,4,2 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 226420-39:
(8*2)+(7*2)+(6*6)+(5*4)+(4*2)+(3*0)+(2*3)+(1*9)=109
109 % 10 = 9
So 226420-39-9 is a valid CAS Registry Number.

226420-39-9Downstream Products

226420-39-9Relevant articles and documents

Efficient separation of perrhenate as analogue to pertechnetate in nitric acid solution with a DOTA-tetraamide ligand: Solvent extraction, complexation and structure study

Ding, Songdong,Hu, Xiaoyang,Song, Lianjun,Wang, Xueyu,Xiao, Qian,Xu, Haowei,Yang, Xiuying

, (2020)

The two DOTA-tetraamide ligands, DOTAM-n-butyl (1,4,7,10-tetrakis[(N-n-butyl; carbamoyl)methyl]-1,4,7,10-tetraazacyclododecane) and DOTAM-benzyl (1,4,7,10- tetrakis[(N-benzylcarbamoyl)methyl]-1,4,7,10-tetraazacyclododecane), were synthesized and character

Complexes of selected late period lanthanide(III) cations with 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid amide (DOTAM)-alkyl ligands-A new platform for the development of paramagnetic chemical exchange saturation transfer (PARACEST) magnetic resonance imaging (MRI) contrast agents

Elmehriki, Adam A.H.,Milne, Mark,Suchy, Mojmir,Bartha, Robert,Hudson, Robert H.E.

, p. 211 - 219 (2013/05/22)

A series of 18 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid amide (DOTAM)-alkyl derived complexes with selected late lanthanide(III) cations (Dy3+, Tb3+, and Tm3+) has been synthesized; their magnetic properties have been evaluated and compared to those derived from DOTAM. Peralkylation of cyclen with corresponding N-iodoacetyl amines was utilized as the key step in the synthesis. Chemical exchange saturation transfer (CEST) spectra of the complexes have been acquired at 37 C, revealing that Tm3+-derived DOTAM-alkyl complexes possess the most favorable properties as potential paramagnetic chemical exchange saturation transfer (PARACEST) magnetic resonance imaging (MRI) contrast agents.

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