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5,6,8,9,11,12-hexakis(4-tert-butylphenyl)[1,2,5]-selenadiazolo[3,4-b]porphyrazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

888014-94-6

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888014-94-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 888014-94-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,8,0,1 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 888014-94:
(8*8)+(7*8)+(6*8)+(5*0)+(4*1)+(3*4)+(2*9)+(1*4)=206
206 % 10 = 6
So 888014-94-6 is a valid CAS Registry Number.

888014-94-6Downstream Products

888014-94-6Relevant academic research and scientific papers

Synthesis, acid-base properties, and deselenation of 5,6,8,9,11,12- hexakis(4-tert-butylphenyl)[1,2,5]selenadiazolo[3,4-b]porphyrazine

Kozlov,Stuzhin

, p. 913 - 921 (2013/07/26)

Cross cyclotetramerization of bis(4-tert-butylphenyl)fumaronitrile with 1,2,5-selenadiazole-3,4-dicarbonitrile in the presence of magnesium butoxide as template afforded a mixture of magnesium(II) porphyrazine complexes, from which magnesium complex of 5,6,8,9,11,12-hexakis(4-tert-butylphenyl)[1,2,5] selenadiazolo[3,4-b]porphyrazine was isolated by column chromatography and was subjected to demetalation on treatment with trifluoroacetic acid. The free ligand was found to undergo protonation at one meso-nitrogen atom in acid medium and deprotonation of one pyrrole ring to form monoanion by the action of bases. Reductive deselenation of the title compound with formation of vicinal diamino porphyrazine was studied by spectral and kinetic methods, and a mechanism involving two hydrosulfide ions was proposed.

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