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4-benzyl-11-(tert-butylcarboxy)methyl-1,4,8,11-tetraazabicyclo[6.6.2]hexadecane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1314032-93-3

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1314032-93-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1314032-93-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,4,0,3 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1314032-93:
(9*1)+(8*3)+(7*1)+(6*4)+(5*0)+(4*3)+(3*2)+(2*9)+(1*3)=103
103 % 10 = 3
So 1314032-93-3 is a valid CAS Registry Number.

1314032-93-3Downstream Products

1314032-93-3Relevant academic research and scientific papers

Challenges in chelating positron emitting copper isotopes: Tailored synthesis of unsymmetric chelators to form ultra stable complexes

Silversides, Jon D.,Smith, Rachel,Archibald, Stephen J.

, p. 6289 - 6297 (2011/08/02)

The synthesis of chelators that form high stability complexes with copper(ii) isotopes and do not suffer from transchelation in vivo has been a goal for many chemists. Such chelators will facilitate the exploitation of the 64Cu isotope (t1/2 = 12.7 h, β+ (19%); β- (39%); EC (41%)) for positron emission tomography imaging studies, which has a longer half life relative to the more commonly used 18F (t1/2 = 109.8 min) and 11C (t1/2 = 20.4 min) isotopes. One option is the CBTE2A chelator, which has been championed by Weisman, Wong and Anderson, and, more recently, alternate bifunctional chelator (BFC) versions have been synthesised. Improved synthetic methods are required for unsymmetric derivatisation of these chelators to allow more selective biomolecule attachment. This work investigates synthetic routes to form new unsymmetric chelating ligands via stepwise reaction of the bisaminal precursor, determines their X-ray structures and demonstrates cold copper(ii) isotope complex formation.

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