90936-85-9 Usage
Description
1-Pyrenehexanoic acid is a chemical compound that features a pyrene ring and a hexanoic acid group. It belongs to the pyrenecarboxylic acids family, which are widely utilized in photochemistry and fluorescence spectroscopy. 1-Pyrenehexanoic acid serves as a reference standard for assessing chromatographic separation techniques and has been explored for its potential anti-inflammatory and anti-oxidant properties. Furthermore, it has been studied for its capacity to influence lipid metabolism, which makes it a valuable subject for research into metabolic disorders such as obesity and diabetes.
Uses
Used in Analytical Chemistry:
1-Pyrenehexanoic acid is used as a reference standard for evaluating the effectiveness of various chromatographic separation methods, aiding in the development and optimization of analytical techniques.
Used in Photochemistry and Fluorescence Spectroscopy:
As a member of the pyrenecarboxylic acids, 1-Pyrenehexanoic acid is utilized in photochemistry and fluorescence spectroscopy applications, taking advantage of its light-absorbing and light-emitting properties.
Used in Pharmaceutical Research:
1-Pyrenehexanoic acid is used as a subject of study for its potential anti-inflammatory and anti-oxidant properties, which can contribute to the development of new therapeutic agents.
Used in Metabolic Disorders Research:
1-Pyrenehexanoic acid is used in research into metabolic disorders such as obesity and diabetes due to its ability to modulate lipid metabolism, offering insights into the development of treatments for these conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 90936-85-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,9,3 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 90936-85:
(7*9)+(6*0)+(5*9)+(4*3)+(3*6)+(2*8)+(1*5)=159
159 % 10 = 9
So 90936-85-9 is a valid CAS Registry Number.
InChI:InChI=1/C22H20O2/c23-20(24)8-3-1-2-5-15-9-10-18-12-11-16-6-4-7-17-13-14-19(15)22(18)21(16)17/h4,6-7,9-14H,1-3,5,8H2,(H,23,24)
90936-85-9Relevant articles and documents
Ground-State Dimers in Excimer-Forming Bichromophoric Molecules. NMR and Single-Photon-Counting Data: 2. Racemic and Meso Dipyrenylpentanes and Dipyrenylalkanes
Reynders, Peter,Kuehnle, Wolfgang,Zachariasse, Klaas A.
, p. 4073 - 4082 (1990)
1H-NMR spectra of the racemic and meso diastereomers of 2,4-di(1-pyrenyl)pentane (1DPP) in toluene-d8 and of the 1,n-di(1-pyrenyl)alkanes (1Py(n)1Py with n = 0-10 and 13) and 1,n-di(2-pyrenyl)alkanes (2Py(n)2Py with n = 1-10 and 14) in chloroform-d were measured at room temperature.The conformer distribution in both 1DPP molecules was determined from an analysis of the vicinal coupling constants between the methylene and methine protons.In meso-1DPP, an intramolecular sandwichlike ground-state dimer was detected, whereas in rac-1DPPP a dimer only overlapping at the aromatic protons H9 and H10 is formed.The presence of both dimers was confirmed by the time-resolved fluorescence measurements (single-photon counting (SPC)).With the dipyrenylalkanes, an analysis of the chemical shifts of the aromatic protons shows that sandwich dimers are not present.Only in the case of 1Py(3)1Py is partial-overlap dimer detected.These findings are supported by results from SPC measurements.
