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1170669-90-5

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1170669-90-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1170669-90-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,0,6,6 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1170669-90:
(9*1)+(8*1)+(7*7)+(6*0)+(5*6)+(4*6)+(3*9)+(2*9)+(1*0)=165
165 % 10 = 5
So 1170669-90-5 is a valid CAS Registry Number.

1170669-90-5Relevant articles and documents

Development and preliminary evaluation of TFIB, a new bimodal prosthetic group for bioactive molecule labeling

Billaud, Emilie M. F.,Vidal, Aurélien,Vincenot, Amélie,Besse, Sophie,Bouchon, Bernadette,Debiton, Eric,Miot-Noirault, Elisabeth,Miladi, Imen,Rbah-Vidal, Latifa,Auzeloux, Philippe,Chezal, Jean-Michel

, p. 168 - 172 (2015)

The new readily available prosthetic group, tetrafluorophenyl 4-fluoro-3-iodobenzoate (TFIB), designed for both molecular imaging and targeted radionuclide therapy purposes was radiolabeled either with fluorine or iodine radionuclides with excellent radiochemical yields and purities. These radiolabeled tags were conjugated to N,N-diethylethylenediamine to give melanin-targeting radiotracers [125I]9 and [18F]9, which were successfully evaluated by PET and gamma scintigraphic imaging in B16F0 pigmented melanoma-bearing C57BL/6J mice. Then, radiolabeled [125I]/[18F]TFIB was used to tag tumor-targeting peptides (i.e., PEG3[c(RGDyK)]2 and NDP-MSH targeting αvβ3 integrin and MC1R receptors, respectively) in mild conditions and with good radiochemical yields (47-83% d.c.) and purities (>99%). The resulting radiolabeled peptides were assessed both in vitro and by PET imaging in animal models.

The development of phenylethylene dendrons for blue phosphorescent emitters

Lo, Shih-Chun,Harding, Ruth E.,Brightman, Edward,Burn, Paul L.,Samuel, Ifor D. W.

experimental part, p. 3213 - 3227 (2010/05/02)

New high triplet energy dendrons based on 1,2-diphenylethylene with and without 2-ethylhexyloxy surface groups have been developed for deep blue phosphorescent iridium(III) dendrimers. The fac-tris[1-methyl-5-(4-fluoro) phenyl-3-n-propyl-1H-[1,2,4]triazolyl]iridium(III)-cored dendrimers, bearing first generation 1,2-diphenylethylene dendrons on the ligand triazolyl and phenyl rings, were prepared in excellent yields, employing Sonogashira cross-couplings and palladium catalysed hydrogenation as the key synthetic steps. Both dendrimers showed good thermal stability although the flexible nature of the dendrons led to the materials having low glass transition temperatures. Dendrimer 15 (without the surface groups) emitted good blue phosphorescence with a solution photoluminescence quantum yield (PLQY) of 46%, Commission Internationale de l'Eclairage (CIE) co-ordinates of (0.15, 0.14) and photoluminescence peaks at 441 and 468 nm. The solution PLQY was 50% higher than the parent iridium(III) complex showing that the high triplet energy of the diphenylethylene dendrons does not quench the luminescence of the iridium(III) complex core. Dendrimer 34, which has the surface groups, had a film PLQY of 49% and CIE co-ordinates of (0.16, 0.19) with PL peaks at 441 and 469 nm. The Royal Society of Chemistry 2009.

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