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162479-04-1

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162479-04-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 162479-04-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,4,7 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 162479-04:
(8*1)+(7*6)+(6*2)+(5*4)+(4*7)+(3*9)+(2*0)+(1*4)=141
141 % 10 = 1
So 162479-04-1 is a valid CAS Registry Number.

162479-04-1Relevant articles and documents

Bisporphyrin connected by pyrimidine: Synthesis and photo physical properties

Achelle, Sylvain,Saettel, Nicolas,Baldeck, Patrice,Fichou, Marie-Paule Teulade,Maillard, Philippe

, p. 877 - 884 (2010)

We report the synthesis of a series of zinc porphyrins conjugated with pyrimidine derivatives. V shaped porphyrin dimer with a pyrimidine central core exhibits a planar geometry according to DFT computational studies, presents an internal charge transfer upon excitation proved by typical solvatochromic behavior and moderate two-photon absorption properties. Such porphyrin conjugates can afford valuable advantages in applications of TPA materials such as in photodynamic therapy and imaging of biological entities.

Central zinc metal-controlled regioselective: meso -bromination of zincated β-silylporphyrins - rapid access to meso,β-dual-functionalized porphyrins

Hayashi, Satoshi,Takamatsu, Rina,Takeda, Shiori,Noji, Masahiro,Takanami, Toshikatsu

, p. 9791 - 9795 (2020)

A convenient method for the preparation of meso,β-dual-functionalized porphyrin was developed. The bromination of zincated β-silylporphyrin with NBS selectively yielded meso-bromo-β-silylporphyrin, whereas, the bromination of free-base β-silylporphyrin selectively yielded β-bromoporphyrin via an ipso-substitution of the silyl group. These meso,β-dual-functionalized porphyrins could be used as multipurpose synthons for fabricating various porphyrin derivatives. This journal is

Porphyrin dimers and arrays

Ryan, Aoife,Gehrold, Andreas,Perusitti, Romain,Pintea, Monica,Fazekas, Marijana,Locos, Oliver B.,Blaikie, Frances,Senge, Mathias O.

experimental part, p. 5817 - 5844 (2011/11/29)

Current applications of porphyrins in medicine and optics, such as photodynamic therapy or nonlinear absorbers, increasingly require the use of far-red absorbing dyes. Modifications of the porphyrin structure to accommodate these conditions can be achieve

Synthesis and ligand binding properties of triptycene-linked porphyrin arrays

Finnigan, Eimear M.,Rein, Regis,Solladié, Nathalie,Dahms, Katja,G?tz, Daniel C.G.,Bringmann, Gerhard,Senge, Mathias O.

body text, p. 1126 - 1134 (2011/03/22)

Multiporphyrin arrays are a complex class of molecules with numerous potential applications in energy transfer, photomedicine, and light harvesting. We have developed a facile/versatile route to a class of triptycene-linked porphyrin arrays via both Suzuk

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