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2,6-bis-[2-(3,4-dihydroxyphenyl)ethyl]pyrrolo[3,4-f]isoindole-1,3,5,7-tetrone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1263218-33-2

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1263218-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1263218-33-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,3,2,1 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1263218-33:
(9*1)+(8*2)+(7*6)+(6*3)+(5*2)+(4*1)+(3*8)+(2*3)+(1*3)=132
132 % 10 = 2
So 1263218-33-2 is a valid CAS Registry Number.

1263218-33-2Downstream Products

1263218-33-2Relevant academic research and scientific papers

Structural study on solvates of dopamine-based cyclic imide derivatives

Singh, Devendra,Baruah, Jubaraj B.

, p. 768 - 777 (2011)

A structural study on two dopamine-based imide derivatives, namely, 2-(3,4-dihydroxyphenethyl)isoindole-1,3-dione (1) and 2,6-bis-[2-(3,4- dihydroxyphenyl)ethyl]pyrrolo [3,4-f]isoindole-1,3,5,7-tetrone (2), and their solvates was carried out. The compound 1 (Z′ = 2) was crystallized through a melt crystallization process, whereas its two solvates (Z′ = 1 of each), containing one water molecule (1a) and the other containing two quinoline molecules (1b) in their crystal lattices, respectively, were obtained through solution crystallization. The reasons for Z′ = 2 arising from symmetry nonequivalent molecules in the unit cell of 1 is attributed to the nonparallel arrangement of two layers of self-assembled molecules in crystal lattice, where one layer has C-H???π and another layer has C=O???π interactions. Four different solvates of compound 2 (Z′ = 0.5 of each), containing two DMF molecules (2a), two DMSO molecules (2b), two pyridine molecules (2c), and six quinoline molecules (2d), were also obtained through solution crystallization of 2 in respective solvents. Solvate 2d has channels in its structure which are formed by interaction of 2 with quinoline molecules through O-H???N and C-H???π interactions. Additional quinoline molecules reside in these channels of approximately (11 × 12) A dimension. Structural features of all the compounds and their solvates have been studied by single crystal X-ray structures, powder X-ray diffractions (PXRD), thermogravimetric analyses (TGA), and differential scanning calorimetric (DSC) measurements.

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