Rel-(2R,3S)-2,3-Bis(chloromethyl)oxirane, with the CAS number 50703-46-3, is a chiral epoxide compound characterized by the presence of two chloromethyl groups attached to a three-membered oxirane ring. This compound exhibits a unique stereochemistry, as indicated by its (2R,3S) configuration, which influences its reactivity and potential applications in organic synthesis. The chloromethyl groups enhance its electrophilic character, making it a useful intermediate in various chemical reactions, including nucleophilic substitutions and ring-opening reactions. The oxirane structure contributes to its strain and reactivity, allowing it to participate in diverse chemical transformations. Additionally, the compound's physical properties, such as boiling point and solubility, are influenced by the presence of the chloromethyl groups and the oxirane ring. Due to its specific stereochemistry and functional groups, this compound may find applications in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals, where precise control over stereochemistry is essential. Safety precautions should be taken when handling this compound, as it may pose health and environmental risks.

rel-(2R,3S)-2,3-Bis(chloromethyl)oxirane

50703-46-3: Rel-(2R,3S)-2,3-Bis(chloromethyl)oxirane, with the CAS number 50703-46-3, is a chiral epoxide compound characterized by the presence of two chloromethyl groups attached to a three-membered oxirane ring. This compound exhibits a unique stereochemistry, as indicated by its (2R,3S) configuration, which influences its reactivity and potential applications in organic synthesis. The chloromethyl groups enhance its electrophilic character, making it a useful intermediate in various chemical reactions, including nucleophilic substitutions and ring-opening reactions. The oxirane structure contributes to its strain and reactivity, allowing it to participate in diverse chemical transformations. Additionally, the compound's physical properties, such as boiling point and solubility, are influenced by the presence of the chloromethyl groups and the oxirane ring. Due to its specific stereochemistry and functional groups, this compound may find applications in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals, where precise control over stereochemistry is essential. Safety precautions should be taken when handling this compound, as it may pose health and environmental risks.

CAS 50703-46-3

rel-(2R,3S)-2,3-Bis(chloromethyl)oxirane

rac-(2R,3S)-2,3-Bis(chloromethyl)oxirane

Ref: 3D-ACA70346