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2-Phenylquinoline is an organic compound with the chemical formula C15H11N. It is a derivative of quinoline, a heterocyclic aromatic compound, and features a phenyl group (C6H5) attached to the 2-position of the quinoline ring. This molecule is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and properties. It is also used as an intermediate in the production of dyes and pigments. 2-Phenylquinoline is characterized by its yellow crystalline appearance and is insoluble in water but soluble in organic solvents. Its chemical properties include the ability to undergo electrophilic substitution reactions due to the presence of the phenyl group, which can influence the reactivity of the quinoline nucleus.

612-73-7

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612-73-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 612-73-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 612-73:
(5*6)+(4*1)+(3*2)+(2*7)+(1*3)=57
57 % 10 = 7
So 612-73-7 is a valid CAS Registry Number.

612-73-7Upstream product

612-73-7Downstream Products

612-73-7Relevant academic research and scientific papers

Synthesis and characterization of a deuterium labeled stercobilin: A potential biomarker for autism

Coffey, Jordan M.,Vadas, Andrew J.,Puleo, Thomas R.,Lewis, Katelyn P.,Pirrone, Gregory F.,Rudolph, Heather L.,Helms, Eric D.,Wood, Troy D.,Flynn-Charlebois, Amber

, p. 742 - 748 (2018/08/21)

Stercobilin is an end-stage metabolite of hemoglobin, a component of red blood cells. It has been found that there is a significantly lower concentration of stercobilin in the urine of people diagnosed with autism spectrum disorders, suggesting potential use as a biomarker. In vitro, we have synthesized stercobilin from its precursor bilirubin through a reduction reaction proceeded by an oxidation reaction. In addition, we have isotopically labeled the stercobilin product with deuterium using this protocol. Nuclear magnetic resonance investigations show the products of the unlabeled stercobilin (Rxn 1) and the deuterated stercobilin (Rxn 2) both had a loss of signals in the 5.0- to 7.0-ppm range indicating proper conversion to stercobilin. Changes in the multiplicity of the sp3 region of the proton nuclear magnetic resonance suggest proper deuterium incorporation. Mass spectrometry studies of Rxn 1 show a difference in fragmentation patterns than that of Rxn 2 proposing potential locations for deuterium incorporation. This isotopologue of stercobilin is stable (>6?mo), and further analysis permits investigation for its use as a biomarker and potential quantitative diagnostic probe for autism spectrum disorders.

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