(2R)-2-(Fluoromethyl)oxirane, also known as a fluorinated epoxide, is a chemical compound characterized by its three-membered cyclic ether structure, which includes an epoxide functional group. The presence of a fluoromethyl group at the second carbon atom contributes to its unique reactivity and properties. This compound is typically colorless and may be volatile, with a relatively low boiling point compared to larger organic molecules. Its fluorine atom enhances its polarity and can influence its solubility in various solvents, making it useful in organic synthesis and as an intermediate in the production of pharmaceuticals and agrochemicals. The stereochemistry indicated by the (2R) designation suggests that the compound has specific spatial arrangements that can affect its biological activity and interaction with other molecules. Additionally, the presence of the epoxide group makes it reactive towards nucleophiles, allowing for further chemical transformations. Safety precautions should be taken when handling this compound due to its potential reactivity and toxicity.

(2R)-2-(Fluoromethyl)oxirane

83398-56-5: (2R)-2-(Fluoromethyl)oxirane, also known as a fluorinated epoxide, is a chemical compound characterized by its three-membered cyclic ether structure, which includes an epoxide functional group. The presence of a fluoromethyl group at the second carbon atom contributes to its unique reactivity and properties. This compound is typically colorless and may be volatile, with a relatively low boiling point compared to larger organic molecules. Its fluorine atom enhances its polarity and can influence its solubility in various solvents, making it useful in organic synthesis and as an intermediate in the production of pharmaceuticals and agrochemicals. The stereochemistry indicated by the (2R) designation suggests that the compound has specific spatial arrangements that can affect its biological activity and interaction with other molecules. Additionally, the presence of the epoxide group makes it reactive towards nucleophiles, allowing for further chemical transformations. Safety precautions should be taken when handling this compound due to its potential reactivity and toxicity.

CAS 83398-56-5

(2R)-2-(Fluoromethyl)oxirane