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5,5'-(1,3-phenylenebis(methylene))bis(oxy)diisophthalic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

147566-76-5

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147566-76-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147566-76-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,5,6 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 147566-76:
(8*1)+(7*4)+(6*7)+(5*5)+(4*6)+(3*6)+(2*7)+(1*6)=165
165 % 10 = 5
So 147566-76-5 is a valid CAS Registry Number.

147566-76-5Downstream Products

147566-76-5Relevant academic research and scientific papers

Versatile Assembly of Metal-Coordinated Calix[4]resorcinarene Cavitands and Cages through Ancillary Linker Tuning

Pei, Wen-Yuan,Xu, Guohai,Yang, Jin,Wu, Hui,Chen, Banglin,Zhou, Wei,Ma, Jian-Fang

, p. 7648 - 7656 (2017)

We propose a design strategy for assembly of metal-coordinated calix[4]resorcinarene cavitands and cages by tuning of the ancillary linkers. Assembly of newly functionalized cavitand with angular isophthalic acid analogs affords three intriguing metal-coordinated cavitands with deep cavities, 1a-1c. Further, by mediating appropriate spacers between two isophthalic acids, two bowl-shaped cavitands are successfully joined together to produce three elegant coordination cages with tunable sizes and shapes, 2a-2c. The cavitand and cage crystals possess considerable amount of accessible porosities, as clearly established by gas adsorption measurements. Remarkably, 1a-1c also exhibit high structural flexibilities, reversibly transforming between the open-pore and the narrow-pore structures, upon removal and sorption of guest molecules, as evidenced by diffraction and gas adsorption measurements. By combining experimental studies with density functional theory (DFT) calculations, we thoroughly elucidated the mechanism of the structural transformations in response to external stimuli in this new class of flexible porous solids.

Synthesis and characterization of 'picnic-basket' porphyrins with a substituent in the interior of the pocket

Michida,Kyuhara,Nishiyama,Yoshimi,Fitzgerald,Sayo

, p. 3157 - 3162 (2007/10/02)

'Picnic-basket' porphyrins of a new type, that have a substituent in the interior of the pocket, were synthesized to study stabilization of the bound oxygen in hemoprotein models. Though these Co(II) porphyrins have enormous equilibrium constants for the formation of base adducts, hydrogen-bonding interaction with coordinated dioxygen is not as effective for stabilization of the metal-dioxygen bond as we had expected. The results suggest that doming of the porphyrin plane plays an important role in the binding of dioxygen.

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