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1360944-93-9

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1360944-93-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1360944-93-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,0,9,4 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1360944-93:
(9*1)+(8*3)+(7*6)+(6*0)+(5*9)+(4*4)+(3*4)+(2*9)+(1*3)=169
169 % 10 = 9
So 1360944-93-9 is a valid CAS Registry Number.

1360944-93-9Downstream Products

1360944-93-9Relevant academic research and scientific papers

Modular Synthetic Route to Monofunctionalized Porphyrin Architectures

Heitmann, Gernot,Dommaschk, Marcel,L?w, Roland,Herges, Rainer

, p. 5228 - 5231 (2016)

The synthesis of a borylated Ni2+ porphyrin and its application as a versatile precursor for building up functional ortho-substituted tetraaryl porphyrin architectures is reported. This precursor porphyrin provides the basis for efficient modul

Photoswitchable Magnetic Resonance Imaging Contrast by Improved Light-Driven Coordination-Induced Spin State Switch

Dommaschk, Marcel,Peters, Morten,Gutzeit, Florian,Schütt, Christian,N?ther, Christian,S?nnichsen, Frank D.,Tiwari, Sanjay,Riedel, Christian,Boretius, Susann,Herges, Rainer

, p. 7552 - 7555 (2015/07/02)

We present a fully reversible and highly efficient on-off photoswitching of magnetic resonance imaging (MRI) contrast with green (500 nm) and violet-blue (435 nm) light. The contrast change is based on intramolecular light-driven coordination-induced spin state switch (LD-CISSS), performed with azopyridine-substituted Ni-porphyrins. The relaxation time of the solvent protons in 3 mM solutions of the azoporphyrins in DMSO was switched between 3.5 and 1.7 s. The relaxivity of the contrast agent changes by a factor of 6.7. No fatigue or side reaction was observed, even after >100 000 switching cycles in air at room temperature. Electron-donating substituents at the pyridine improve the LD-CISSS in two ways: better photostationary states are achieved, and intramolecular binding is enhanced.

Single azopyridine-substituted porphyrin molecules for configurational and electronic switching

Matino, Francesca,Schull, Guillaume,Jana, Umasish,Koehler, Felix,Berndt, Richard,Herges, Rainer

supporting information; experimental part, p. 6780 - 6782 (2010/11/04)

A new azopyridine functionalized Ni-porphyrin was synthesized as a model compound for deposition and switch on surfaces. Two geometrically and electronically different states of single molecules on Au(111) were found by scanning tunneling microscopy/spectroscopy and analyzed with density functional calculations.

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