207613-06-7 Usage
General Description
N-(carboxymethyl)-N-[3-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)propyl]-D-glucamine is a chemical compound that is used for its chelating and sequestering properties. It is commonly used as a corrosion inhibitor in metal treatment processes and as a sequestrant in various industrial processes and consumer products. N-(carboxymethyl)-N-[3-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl) is effective at binding and removing metal ions, which helps to prevent corrosion and scale formation in industrial equipment and water systems. It is also used in the production of detergents, cleaners, and personal care products as a builder and water softener. Additionally, it has been studied for its potential as a drug delivery agent and in medical imaging applications.
Check Digit Verification of cas no
The CAS Registry Mumber 207613-06-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,6,1 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 207613-06:
(8*2)+(7*0)+(6*7)+(5*6)+(4*1)+(3*3)+(2*0)+(1*6)=107
107 % 10 = 7
So 207613-06-7 is a valid CAS Registry Number.
207613-06-7Relevant articles and documents
Site directed maleimide bifunctional chelators for the M(CO) 3+ core (M = 99mTc, Re)
Banerjee, Sangeeta Ray,Babich, John W.,Zubieta, Jon
, p. 1784 - 1786 (2005)
A series of bifunctional chelates containing a tridentate donor set for complexation of the M(CO)3+ core and a maleimide group for site-specific coupling to peptides and proteins containing free thiol groups has been prepared and their Re(CO)3+ complexes and glutathione conjugates structurally characterized. The flexibility of design allows preparation of ligands suitable for both fluorescence imaging, radioimaging and radiotherapeutic studies of proteins and peptides as well as other biopolymers using site specific conjugation. The Royal Society of Chemistry 2005.
