173276-82-9 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 10 carbon (C) atoms, 7 hydrogen (H) atoms, 1 fluorine (F) atom, and 1 oxygen (O) atom.
Explanation
1,4-Epoxynaphthalene,6-fluoro-1,4-dihydro-(9CI) is derived from naphthalene, which is a polycyclic aromatic hydrocarbon consisting of two fused benzene rings.
Explanation
The compound contains a fluorine atom, which can impart specific properties to the molecule, making it useful for various applications in the chemical and pharmaceutical industries.
Explanation
Epoxides are a type of cyclic ether, characterized by a three-membered ring consisting of two carbon atoms and one oxygen atom. In this case, the oxygen atom is part of the epoxy ring.
Explanation
Due to its unique structure and properties, 1,4-Epoxynaphthalene,6-fluoro-1,4-dihydro-(9CI) is widely used in various industries, including organic synthesis, the production of plastics, pharmaceuticals, and pesticides.
Explanation
As with any chemical compound, proper handling and safety precautions should be taken to avoid potential hazards associated with its use. This includes wearing appropriate personal protective equipment (PPE) and following established safety protocols.
Explanation
The presence of the fluorine atom in the compound can influence its reactivity, making it more or less reactive than other naphthalene derivatives. This can be useful for specific applications in the chemical and pharmaceutical industries.
Explanation
The stability of the compound can be affected by the presence of the fluorine atom, which can alter its resistance to degradation or decomposition under certain conditions.
Explanation
The solubility of 1,4-Epoxynaphthalene,6-fluoro-1,4-dihydro-(9CI) can depend on the solvent used, with some solvents being more effective at dissolving the compound than others.
Explanation
The boiling point of the compound is not mentioned in the provided material, but it can be an important property for determining its suitability for specific applications or processes.
Derivative of Naphthalene
Yes
Fluorine Atom
Present
Classification
Epoxide
Applications
Organic Synthesis, Plastics, Pharmaceuticals, and Pesticides
Safety Precautions
Required
Reactivity
Can vary depending on the presence of the fluorine atom
Stability
Can be influenced by the fluorine atom
Solubility
Can vary depending on the solvent
Boiling Point
Not provided in the material
Check Digit Verification of cas no
The CAS Registry Mumber 173276-82-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,2,7 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 173276-82:
(8*1)+(7*7)+(6*3)+(5*2)+(4*7)+(3*6)+(2*8)+(1*2)=149
149 % 10 = 9
So 173276-82-9 is a valid CAS Registry Number.
173276-82-9Relevant articles and documents
Structural modifications of nile red carbon monoxide fluorescent probe: Sensing mechanism and applications
Klán, Petr,Madea, Dominik,Martínek, Marek,Muchová, Lucie,Váňa, Ji?í,Vítek, Libor
, p. 3473 - 3489 (2020/03/25)
Carbon monoxide (CO) is a cell-signaling molecule (gasotransmitter) produced endogenously by oxidative catabolism of heme, and the understanding of its spatial and temporal sensing at the cellular level is still an open challenge. Synthesis, optical properties, and study of the sensing mechanism of Nile red Pd-based CO chemosensors, structurally modified by core and bridge substituents, in methanol and aqueous solutions are reported in this work. The sensing fluorescence "off-on" response of palladacycle-based sensors possessing low-background fluorescence arises from their reaction with CO to release the corresponding highly fluorescent Nile red derivatives in the final step. Our mechanistic study showed that electron-withdrawing and electron-donating core substituents affect the rate-determining step of the reaction. More importantly, the substituents were found to have a substantial effect on the Nile red sensor fluorescence quantum yields, hereby defining the sensing detection limit. The highest overall fluorescence and sensing rate enhancements were found for a 2-hydroxy palladacycle derivative, which was used in subsequent biological studies on mouse hepatoma cells as it easily crosses the cell membrane and qualitatively traces the localization of CO within the intracellular compartment with the linear quantitative response to increasing CO concentrations.
A Selective C?H Deprotonation Strategy to Access Functionalized Arynes by Using Hypervalent Iodine
Sundalam, Sunil K.,Nilova, Aleksandra,Seidl, Thomas L.,Stuart, David R.
, p. 8431 - 8434 (2016/07/19)
Described here is an efficient method to access highly functionalized arynes from unsymmetrical aryl(mesityl)iodonium tosylate salts. The iodonium salts are prepared in a single pot from either commercially available aryl iodides or arylboronic acids. The
Synthesis of monofluorinated 1-(naphthalen-1-yl)piperazines
Repine, Joseph T.,Johnson, Douglas S.,White, Andrew D.,Favor, David A.,Stier, Michael A.,Yip, Judy,Rankin, Trent,Ding, Qizhu,Maiti, Samarendra N.
, p. 5539 - 5541 (2008/02/13)
A series of regioisomerically monofluorinated 1-(naphthalen-1-yl)piperazines is described.
