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bis(4-ethyl-3-methyl-2-pyrryl)(4-(hydroxymethyl)phenyl)methane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

129618-97-9

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129618-97-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129618-97-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,6,1 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 129618-97:
(8*1)+(7*2)+(6*9)+(5*6)+(4*1)+(3*8)+(2*9)+(1*7)=159
159 % 10 = 9
So 129618-97-9 is a valid CAS Registry Number.

129618-97-9Relevant academic research and scientific papers

Synthesis, self-assembling properties and incorporation of carbohydrate-substituted porphyrins into cell membrane models

Schell, Christian,Hombrecher, Hermann K.

, p. 587 - 598 (2007/10/03)

A general and very efficient synthesis of new carbohydrate-substituted porphyrins is described. Reaction of porphyrin 6 with different glycosyl imidates 7a-g leads to the formation of carbohydrate-substituted porphyrins 9a-g in good yield. Subsequent demetallation and removal of the carbohydrate protection groups leads to the metal-free compounds 11a-g. In aqueous solution, compounds 11a-g tend to form defined water-soluble aggregates in a self-assembling process. In methanol/water mixtures the aggregation process depends upon the configuration of the anomeric carbon in the carbohydrate moiety. The porphyrinic aggregates are characterized by strong exciton splitting in the Soret absorption spectrum and a red shift for all absorption bands. Interaction of the porphyrinic aggregates with phosphatidylethanolamine and DMPC liposomes leads to very efficient incorporation of mainly monomeric porphyrins 11a-g into the liposomes, as was indicated by very large binding constants. At low liposome concentrations noncovalent porphyrin dimers were detected.

Electronic energy migration and trapping in quinone-substituted, phenyl-linked dimeric and trimeric porphyrins

Sessler, Jonathan L.,Capuano, Vincent L.,Harriman, Anthony

, p. 4618 - 4628 (2007/10/02)

The synthesis and photophysical characterization of a series of quinone-substituted, phenyl-linked dimeric and trimeric porphyrin arrays suitable for the study of electron transfer within closely-coupled subunits is presented. The excited singlet state of

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