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2,3-Nitro-p-quaterphenyl is an organic compound with the molecular formula C20H13N3O4. It is a derivative of p-quaterphenyl, a polycyclic aromatic hydrocarbon consisting of four fused benzene rings. The compound is characterized by the presence of a nitro group (-NO2) at the 2nd and 3rd carbon positions, which imparts a yellow color to the solid. 2,3-Nitro-p-quaterphenyl is known for its potential applications in the synthesis of various dyes, pigments, and pharmaceuticals. Due to its complex structure and reactive functional groups, it is also of interest in the field of materials science and organic chemistry research.

2499-74-3

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2499-74-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2499-74-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,9 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2499-74:
(6*2)+(5*4)+(4*9)+(3*9)+(2*7)+(1*4)=113
113 % 10 = 3
So 2499-74-3 is a valid CAS Registry Number.

2499-74-3Downstream Products

2499-74-3Relevant academic research and scientific papers

Multicomponent Crystals with Two Fast Reorienting Constituents over Perpendicular Noncovalent Axes

Colin-Molina, Abraham,Arcudia, Jessica,López-López, Eliseo R.,Jellen, Marcus J.,García-González, Ma. Carmen,Merino, Gabriel,Rodríguez-Molina, Braulio

, p. 673 - 680 (2022/01/03)

Here, we report two new multicomponent crystals (1 and 2) using 2,7-diphenyl-9H-carbazole as the static fragment and two highly mobile components: 1,4-diazabicyclo[2.2.2]octane (DABCO) and tetrahydrofuran (THF). Our findings indicate that their motion does not take place in an isotropic and multiaxial manner, as it occurs in many inclusion compounds, but rather, two independent hydrogen bonds act as specific rotational axes within the crystals. Highly symmetric DABCO rotates over an N-H···N axis, while THF preferentially rotates around a weak C-H···O axis that is perpendicular to that of DABCO. Dynamic characterization of 1 by VT 2H NMR experiments supports that DABCO experiences rapid jumps of 120° (threefold) with a krot > 10 MHz at 300 K and 5 MHz at 150 K. At the same time, THF experiences 180° jumps in the fast regime, even at 175 K. Complementarily, 1H(T1) relaxometry studies show that DABCO has an Ea = 3.5 kcal/mol, while for THF, an Ea = 2.3 kcal/mol was computed by periodic DFT. Non-isotropic mobility of two constituents within crystals is extremely rare and could have strong implications for future applications of multicomponent solids with regulated dynamics.

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