85579-27-7 Usage
Explanation
The compound is composed of 8 carbon atoms, 6 hydrogen atoms, 2 nitrogen atoms, 2 oxygen atoms, and 1 sulfur atom.
Explanation
The core of the molecule is a pentalene ring, which is a five-membered ring with alternating double and single bonds.
Explanation
The compound contains two oxygen atoms, two nitrogen atoms, and one sulfur atom, which are distributed throughout the molecule and contribute to its unique properties.
Explanation
The compound features a dioxolane (cyclic ether), diazine (six-membered ring with two nitrogen atoms), and dithia (two sulfur atoms bonded to each other) functional groups.
Explanation
The pentalene ring exhibits partial aromaticity due to the presence of alternating double and single bonds.
Explanation
The unique arrangement of heteroatoms and functional groups in the compound makes it a promising candidate for various applications in these fields.
Explanation
The compound's intricate structure, with multiple heteroatoms and functional groups, makes it a fascinating subject for study and potential use in scientific and industrial applications.
Explanation
The presence of multiple heteroatoms and functional groups in the molecule contributes to its stability, making it suitable for various applications.
Explanation
The compound's reactivity depends on the specific functional groups and heteroatoms present, which can participate in various chemical reactions.
Explanation
Due to its nonpolar nature and the presence of multiple heteroatoms, the compound is likely to be soluble in organic solvents such as dichloromethane, ethyl acetate, or acetone.
Central ring structure
Pentalene
Heteroatoms
Oxygen, Nitrogen, and Sulfur
Functional groups
Dioxolane, Diazine, and Dithia
Aromaticity
Partially aromatic
Potential applications
Materials science, organic synthesis, and medicinal chemistry
Complex structure
Highly functionalized
Stability
Moderate to high
Reactivity
Variable
Solubility
Soluble in organic solvents
Check Digit Verification of cas no
The CAS Registry Mumber 85579-27-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,5,7 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 85579-27:
(7*8)+(6*5)+(5*5)+(4*7)+(3*9)+(2*2)+(1*7)=177
177 % 10 = 7
So 85579-27-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H4N2O4S2/c8-13(9)1-3-5-4(2-13)7-11-12(5)10-6-3/h1-2H2
85579-27-7Relevant academic research and scientific papers
The Synthesis and Electrochemical Properties of Some Novel Photosynthesis Electron Acceptors
Camilleri, Patrick,Clark, Michael T.,Gilmore, Ian J.,Cole-Hamilton, David
, p. 833 - 836 (2007/10/02)
A range of dioxathiadiaza heteropentalenes have been prepared and their electrochemical properties have been studied by cyclic voltammetry and e.s.r. spectroscopy.It has been found that these compounds form stable anion radicals in the absence of oxygen and have half-peak reduction potentials in the same range as the bypyridinium compounds such as paraquat (methyl viologen) or diquat.
Electrochemical properties of 1-Oxa-6,6aλ4-dithia-2,5-diazapentalene
Patrick, Camilleri,Gilmore, Ian J.,Cole-Hamilton, David J.
, p. 1797 - 1800 (2007/10/02)
The electrochemical propeties of a number of 1-oxa-6,6aλ4-dithia-2,5-diazapentalenes have been studied by cyclovoltammetry and e.s.r. spectroscopy.In general, these compounds have half-peak reduction potentials in the range -380 to -540 mV (vs.Ag-AgCl).The reduction of these heterapentalenes leads to the formation of stable anion radicals, the e.s.r. spectra of which have been characterised.
