2,3,5,6-TETRAFLUOROBENZOYLCHLORIDE CAS:107535-73-9
Catalog Number | XD95691 |
Product Name | 2,3,5,6-TETRAFLUOROBENZOYLCHLORIDE |
CAS | 107535-73-9 |
Molecular Formula | C7HClF4O |
Molecular Weight | 212.53 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
2,3,5,6-Tetrafluorobenzoylchloride is a chemical compound with the molecular formula C7HClF4O. It belongs to the class of benzoyl chlorides, and its structure is characterized by the presence of four fluorine atoms and one chlorine atom on the benzene ring. This unique combination of atoms gives 2,3,5,6-Tetrafluorobenzoylchloride several effects and properties. Below are some of the notable effects of this compound:Reactivity: The presence of both fluorine and chlorine atoms on the benzene ring makes 2,3,5,6-Tetrafluorobenzoylchloride highly reactive. It can undergo various chemical reactions including acylations, chlorinations, and synthetic transformations. This reactivity makes it a valuable compound in organic synthesis for the preparation of diverse compounds.Electrophilic Nature: Due to the presence of electron-withdrawing fluorine and chlorine atoms, 2,3,5,6-Tetrafluorobenzoylchloride is highly electron deficient. This makes it an effective electrophile, meaning it readily accepts electron pairs from other compounds. This electrophilicity is advantageous in a range of reactions, including nucleophilic substitutions and additions.Strong Acidic Properties: The chlorine atom attached to the carbonyl group in 2,3,5,6-Tetrafluorobenzoylchloride makes it an acidic compound. The acidity can be attributed to the polar nature of the C-Cl bond and the withdraw of electron density from the carbonyl carbon. The compound can act as a source of protons or as a catalyst in acid-catalyzed reactions.Solvent and Chemical Compatibility: 2,3,5,6-Tetrafluorobenzoylchloride is sparingly soluble or insoluble in water due to its hydrophobic nature. However, it is readily soluble in many organic solvents such as dichloromethane, chloroform, and ether. This solubility enables its use in various organic reactions and as a reagent in organic synthesis.Safety Considerations: 2,3,5,6-Tetrafluorobenzoylchloride is a hazardous compound and should be handled with caution. It is corrosive to the skin, eyes, and respiratory system. Proper protective equipment, such as gloves, safety glasses, and a fume hood, should be used when working with this compound.In summary, 2,3,5,6-Tetrafluorobenzoylchloride shows significant effects and properties due to its reactivity, electrophilicity, acidic nature, and solvent compatibility. Its reactivity and electrophilicity make it useful in various organic synthesis processes, while its acidic properties enable it to facilitate acid-catalyzed reactions. However, safety precautions must be followed when handling this compound to avoid potential hazards.