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1006711-90-5

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  • 2,2',2''-(10-(2-((2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)ethyl)amino)-2-oxoethyl)-1,4,7,10-tetraazacyclododecane-1,4,7-triyl)triacetic acid

    Cas No: 1006711-90-5

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1006711-90-5 Usage

Use in medicine

Chelating agent
It is used in the field of medicine to bind with metal ions in the body.

Derived from

EDTA (ethylenediaminetetraacetic acid)
A derivative of the chelating agent EDTA, which is a widely used compound in various applications.

Function

Removal of metal ions from the bloodstream
Helps to remove metal ions from the bloodstream, which can be useful in treating heavy metal poisoning and certain medical imaging procedures.

Composition

Multiple nitrogen and oxygen atoms
Contains multiple nitrogen and oxygen atoms that allow it to form stable complexes with a variety of metal ions.

Structure

Complex
The compound has a complex structure, which contributes to its suitability for various applications in medicine and biochemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1006711-90-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,6,7,1 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1006711-90:
(9*1)+(8*0)+(7*0)+(6*6)+(5*7)+(4*1)+(3*1)+(2*9)+(1*0)=105
105 % 10 = 5
So 1006711-90-5 is a valid CAS Registry Number.

1006711-90-5Downstream Products

1006711-90-5Relevant articles and documents

Conjugates of the B-subunit of shiga toxin for use as contrasting agents for imaging and therapy

-

, (2014/06/24)

Multivalent conjugates comprising the following formula: (STxB-linker A-S)x-GNS-(S-linker B-T)y wherein STxB is the B-subunit of Shiga toxin; linker A is a noncleavable linker; linker B is a cleavable linker used to release at least

Bifunctional ligands based on the DOTA-monoamide cage

Barge, Alessandro,Tei, Lorenzo,Upadhyaya, Dharita,Fedeli, Franco,Beltrami, Lorena,Stefania, Rachele,Aime, Silvio,Cravotto, Giancarlo

experimental part, p. 1176 - 1184 (2008/10/09)

Efficient routes to DOTA-monoamide ligands bearing amino, hydroxyl, aldehyde and maleimido groups are described. These functional groups, which can be spaced at will from the coordination cage, will readily react with suitable groups of targeting moieties

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