76492-96-1 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 4 carbon (C), 4 hydrogen (H), 4 fluorine (F), and 2 oxygen (O) atoms.
Explanation
These are alternative names used to refer to the same chemical compound, which can be helpful for identification and communication purposes.
Explanation
Organofluorine compounds are a class of chemicals that contain carbon-fluorine bonds. 1,3-Dioxolane,4,4,5,5-tetrafluoro-(9CI) falls under this category due to the presence of fluorine atoms bonded to carbon.
Explanation
The compound is used as a solvent in various chemical reactions and is also utilized in the synthesis of pharmaceuticals and agrochemicals due to its unique properties.
Explanation
The compound has a high boiling point, which means it requires a significant amount of heat to change from a liquid to a gas. This property can be useful in certain industrial processes.
Explanation
The compound is stable and does not readily react with other substances under typical conditions, making it suitable for various applications.
Explanation
The compound is flammable, which means it can easily catch fire when exposed to a source of ignition. This property requires special handling and safety precautions to prevent accidents.
Explanation
Exposure to the compound without proper safety measures can pose health hazards, such as respiratory issues or skin irritation. It is crucial to follow safety guidelines and use appropriate protective equipment when handling this chemical.
Explanation
The compound is primarily used in industrial settings for various chemical processes and in research environments for studying its properties and potential applications.
Classification
Organofluorine compound
Applications
Solvent, pharmaceuticals, and agrochemicals production
Boiling point
High
Stability
Stable under normal conditions
Flammability
Flammable
Health hazards
Potential health risks if proper safety measures are not in place
Usage
Industrial applications and research settings
Check Digit Verification of cas no
The CAS Registry Mumber 76492-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,4,9 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 76492-96:
(7*7)+(6*6)+(5*4)+(4*9)+(3*2)+(2*9)+(1*6)=171
171 % 10 = 1
So 76492-96-1 is a valid CAS Registry Number.
76492-96-1Relevant academic research and scientific papers
Muffler, Herbert,Siegemund, Guenter,Schwertfeger, Werner
, p. 107 - 132 (1982)
4.5-Perfluoro-1.3-dioxolanes 2 are available by reaction of 2(α-chloroalkoxy)perfluoro-carbonyl halides 3 or -ketone 9 with fluoride ions.A mechanism for the intramolecular ring-closure-reaction is proposed.Hydrogen atoms at C-2 in 2 can be exchanged photochemically by chlorine.Starting from the 2-monochloro-derivatives 16 the 2-monofluoro-4.5-perfluoro-1.3-dioxolanes 18 are formed by reaction with triethylamine-hydrofluoride.
Process for the preparation of 4,5-perfluoro-1,3-dioxalanes
-
, (2008/06/13)
4,5-Perfluoro-1,3-dioxolanes prepared by the described process have an anesthetic effect.
