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2-(4-(1H-pyrrol-2-yl)phenyl)pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

145654-69-9

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145654-69-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145654-69-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,6,5 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 145654-69:
(8*1)+(7*4)+(6*5)+(5*6)+(4*5)+(3*4)+(2*6)+(1*9)=149
149 % 10 = 9
So 145654-69-9 is a valid CAS Registry Number.

145654-69-9Downstream Products

145654-69-9Relevant academic research and scientific papers

Phototautomerization in Pyrrolylphenylpyridine Terphenyl Systems

Basari?, Nikola,Thomas, Suma S.,Bregovi?, Vesna Bla?ek,Cindro, Nikola,Bohne, Cornelia

, p. 4430 - 4442 (2015/05/13)

[4-(2-Pyrrolyl)phenyl]pyridines 2-4 were synthesized and their photophysical properties and reactivity in phototautomerization reactions investigated by fluorescence spectroscopy and laser flash photolysis (LFP). The pKa for the protonation of the pyridine nitrogen in 2-4 was determined by UV-vis and fluorescence titration (pKa = 5.5 for 4). On excitation in polar protic solvents, 2-4 populate charge-transfer states leading to an enhanced basicity of the pyridine (pKa? ≈ 12) and enhanced acidity of pyrrole (pKa? ≈ 8-9) enabling excited-state proton transfer (ESPT). ESPT gives rise to phototautomers and significantly quenches the fluorescence of 2-4. Phototautomers 2-T and 4-T were detected by LFP with strong transient absorption maxima at 390 nm. Phototautomers 2-T and 4-T decayed by competing uni- and bimolecular reactions. However, at pH 11 the decay of 4-T followed exponential kinetics with a rate constant of 4.2 × 106 s-1. The pyridinium salt 4H+ forms a stable complex with cucurbit[7]uril (CB[7]) with 1:1 stoichiometry (β11 = (1.0 ± 0.2) × 105 M-1, [Na+] = 39 mM). Complexation to CB[7] increased the pKa for 4H+ (pKa = 6.9) and changed its photochemical reactivity. Homolytic cleavage of the pyrrole NH leads to the formation of an N-radical because of the decreased acidity of the pyrrole in the inclusion complex. (Figure Presented).

A simple way to sequentially connected polycycles containing terminal pyrrole rings: Synthesis of possible precursors of materials for nonlinear optics

Lucchesini, Francesco

, p. 9951 - 9966 (2007/10/02)

the readily available 1,3-dioxolane-2-propanal allows the transformation of aromatic and heteroaromatic mono and dilithioderivatives into polycycles containing one or two pyrrole rings. Organolithiums bearing electron acceptor groups can be also employed affording possible precursors of materials for nonlinear optics.

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