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5,10,15-tris(3-hydroxyphenyl)-20-[3-(4-methylphenylsulfonyl)phenyl]porphyrin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1621262-72-3

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1621262-72-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1621262-72-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,1,2,6 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1621262-72:
(9*1)+(8*6)+(7*2)+(6*1)+(5*2)+(4*6)+(3*2)+(2*7)+(1*2)=133
133 % 10 = 3
So 1621262-72-3 is a valid CAS Registry Number.

1621262-72-3Downstream Products

1621262-72-3Relevant academic research and scientific papers

Simple porphyrin desymmetrization: 5,10,15,20-tetrakis(3-hydroxyphenyl) porphyrin (mTHPP) as a gateway molecule for peripheral functionalization

Rogers, Luke,Burke-Murphy, Emeralda,Senge, Mathias O.

, p. 4283 - 4294 (2014/07/21)

The rise in the demand of unsymmetrical porphyrin systems for applications such as photodynamic therapy and nonlinear optics mandates a concomitant development of simple and practical synthetic approaches. A new method for the rapid generation of unsymmetrical porphyrins from the same common and easily accessible symmetric porphyrin starting material is discussed herein. A library of unsymmetric mTHPP [5,10,15,20-tetrakis(3-hydroxyphenyl)porphyrin] derivatives were synthesized in good yields through simple nucleophilic substitution, esterification, and metal-catalyzed cross-coupling reactions. This method was optimized to generate a library of customized unsymmetrical porphyrins quickly for use in a variety of applications. A common meso-aryl-substituted porphyrin as the starting material was used to update the synthetic toolkit through a mixture of classical and modern chemistry. This approach was studied as an approach to the synthesis of picket fence porphyrin mimics and afforded such compounds in good yields with few synthetic steps. In addition, employing simple nucleophilic substitution chemistry was employed to access cofacial caged bis(porphyrin) systems in two synthetic steps. Copyright

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