386-83-4 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 15 carbon (C) atoms, 9 hydrogen (H) atoms, 3 fluorine (F) atoms, and 1 oxygen (O) atom.
Explanation
This describes the specific arrangement of atoms and functional groups in the molecule. The fluorene group is attached to a trifluoroethanone moiety, which is a derivative of a ketone.
Explanation
The compound contains a ketone functional group (C=O), a fluorene aromatic ring system, and a trifluoromethyl group (CF3).
Explanation
The compound is used as a building block or reagent in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and other fluorinated compounds.
Explanation
1-(9H-Fluoren-9-yl)-2,2,2-trifluoroethanone is considered to be a stable chemical, which means it does not readily undergo decomposition or react with other substances under normal conditions.
Explanation
The compound is classified as relatively non-toxic, making it suitable for use in a wide range of chemical reactions and processes without posing significant health or environmental risks.
Explanation
Although the exact physical state is not provided, most organic compounds with a molecular weight similar to 1-(9H-Fluoren-9-yl)-2,2,2-trifluoroethanone are solids or liquids at room temperature.
Explanation
The compound is likely soluble in organic solvents such as dichloromethane, acetone, or ethanol due to its nonpolar nature and the presence of aromatic and fluorinated groups.
Explanation
The compound can participate in various chemical reactions, such as nucleophilic addition, electrophilic substitution, and reduction, due to the presence of its functional groups and aromatic system.
Explanation
The compound is often synthesized with high purity, which is essential for its use in sensitive chemical reactions and the production of pharmaceuticals and agrochemicals.
Chemical Structure
1-(9H-Fluoren-9-yl)-2,2,2-trifluoroethanone
Functional Groups
Ketone, Fluorene, Trifluoromethyl
Application
Organic synthesis, pharmaceuticals, agrochemicals, and fluorinated compounds
Stability
Stable
Toxicity
Relatively non-toxic
Physical State
Likely a solid or liquid at room temperature
Solubility
Soluble in organic solvents
Reactivity
Reacts with various reagents in organic synthesis
Purity
Typically synthesized with high purity
Check Digit Verification of cas no
The CAS Registry Mumber 386-83-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,8 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 386-83:
(5*3)+(4*8)+(3*6)+(2*8)+(1*3)=84
84 % 10 = 4
So 386-83-4 is a valid CAS Registry Number.
