20850-89-9 Usage
Explanation
Different sources of media describe the Explanation of 20850-89-9 differently. You can refer to the following data:
1. The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 14 carbon (C) atoms, 13 hydrogen (H) atoms, 1 oxygen (O) atom, and 2 sulfur (S) atoms.
2. Heterocyclic Compound
2. A heterocyclic compound is a cyclic compound that contains atoms of at least two different elements as members of its ring. In this case, the compound has a dithiolium ring with sulfur and carbon atoms.
3. Dithiolium Ring
3. The dithiolium ring is a part of the compound's structure, consisting of a six-membered ring with two sulfur atoms and four carbon atoms.
4. Hydroxide Group
4. The hydroxide group (OH) is a functional group present in the compound, which contributes to its chemical properties and reactivity.
5. Inner Salt
6. Organic Synthesis
5. The compound is often used in organic synthesis, which is the chemical synthesis of carbon-containing compounds. Its unique structure allows it to participate in various reactions, making it a valuable building block for creating more complex molecules.
7. Ligand in Coordination Chemistry
6. The compound can act as a ligand, which is a molecule that donates a pair of electrons to a central metal atom in a coordination complex. This property allows the compound to form stable complexes with metal ions, which can be useful in various applications.
8. Potential Applications in Pharmaceuticals
7. Due to its unique chemical properties, the compound has potential applications in the development of pharmaceuticals. It may be used as a starting material or a building block for the synthesis of more complex drug molecules.
9. Industrial Processes
8. The compound may also have applications in various industrial processes, such as the synthesis of dyes, pigments, or other specialty chemicals.
10. Biological Activities and Medicinal Chemistry
9. The compound has been studied for its potential biological activities, which may have implications in medicinal chemistry. This means that it could potentially be used as a therapeutic agent or as a lead compound for the development of new drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 20850-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,5 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 20850-89:
(7*2)+(6*0)+(5*8)+(4*5)+(3*0)+(2*8)+(1*9)=99
99 % 10 = 9
So 20850-89-9 is a valid CAS Registry Number.
20850-89-9Relevant articles and documents
Strain-Promoted 1,3-Dithiolium-4-olates–Alkyne Cycloaddition
Kumar, Ramar Arun,Pattanayak, Manas R.,Yen-Pon, Expédite,Eliyan, Jijy,Porte, Karine,Bernard, Sabrina,Riomet, Margaux,Thuéry, Pierre,Audisio, Davide,Taran, Frédéric
, p. 14544 - 14548 (2019/09/17)
Reported here is the reactivity of mesoionic 1,3-dithiolium-4-olates towards strained alkynes, leading to thiophene cycloaddition products. In the process, the potential of these dipoles towards orthogonal reaction with azides, allowing efficient double ligation reactions, was discovered. A versatile process to access benzo[c]thiophenes, in an unprecedented divergent fashion, was developed and provides a new entry to unconventional polyaromatic thiophenes.
Formation of 2,5-diaryl-1,3-dithiolylium-4-olate in thermal reaction of 4-aryl-1,3,2-oxathiazolylium-5-olate
Tono, Masaki,Aoto, Hiroshi,Matsudaira, Yorimasa,Sugiyama, Tom,Kajitani, Masatsugu,Akiyama, Takeo,Sugimori, Akira
, p. 4023 - 4026 (2007/10/02)
The reflux of a meso-ionic compound, 4-aryl-1,3,2-oxathiazolylium-5-olate (1), in toluene, chlorobenzene, or xylene gives another meso-ionic compound, 2,5-diaryl-1,3-dithiolylium-4-olate (2), by a radical mechanism.
