Cyclobutanone-2,2,4,4-d4 is a deuterated form of cyclobutanone, a cyclic ketone with the molecular formula C4H6O. In this specific isotopologue, the hydrogen atoms at positions 2 and 4 of the cyclobutane ring are replaced with deuterium, resulting in a molecular formula of C4D6O. This compound is characterized by its four-membered ring structure, which introduces angle strain due to the bond angles being significantly less than the ideal tetrahedral angle. Cyclobutanone exhibits typical ketone reactivity, including nucleophilic addition and oxidation reactions. Its deuterated nature makes it particularly useful in studies involving nuclear magnetic resonance (NMR) spectroscopy, as the presence of deuterium alters the NMR signals, allowing for detailed analysis of molecular dynamics and interactions. Cyclobutanone-2,2,4,4-d4 is utilized in various fields, including organic synthesis and chemical research, particularly in the study of reaction mechanisms and kinetics. As with many ketones, it is important to handle this compound with care due to potential health hazards associated with inhalation or skin contact.

Cyclobutanone-2,2,4,4-d4

13221-54-0: Cyclobutanone-2,2,4,4-d4 is a deuterated form of cyclobutanone, a cyclic ketone with the molecular formula C4H6O. In this specific isotopologue, the hydrogen atoms at positions 2 and 4 of the cyclobutane ring are replaced with deuterium, resulting in a molecular formula of C4D6O. This compound is characterized by its four-membered ring structure, which introduces angle strain due to the bond angles being significantly less than the ideal tetrahedral angle. Cyclobutanone exhibits typical ketone reactivity, including nucleophilic addition and oxidation reactions. Its deuterated nature makes it particularly useful in studies involving nuclear magnetic resonance (NMR) spectroscopy, as the presence of deuterium alters the NMR signals, allowing for detailed analysis of molecular dynamics and interactions. Cyclobutanone-2,2,4,4-d4 is utilized in various fields, including organic synthesis and chemical research, particularly in the study of reaction mechanisms and kinetics. As with many ketones, it is important to handle this compound with care due to potential health hazards associated with inhalation or skin contact.

CAS 13221-54-0

Cyclobutanone-2,2,4,4-d4

Cyclobutanone-2,2,4,4-d4

Ref: 3U-D8295