3-tert-Butylphenyl chlorothionoformate is an organic compound characterized by its functional groups and structural features. It contains a phenyl ring substituted with a tert-butyl group at the meta position, which contributes to its steric bulk and hydrophobic properties. The chlorothionoformate moiety indicates the presence of a thiocarbonyl group, where a chlorine atom is bonded to a carbon atom that is also double-bonded to sulfur. This structure suggests that the compound may exhibit reactivity typical of thioesters, including potential nucleophilic attack at the carbonyl carbon. The presence of the chlorothionoformate group can also imply that it may be used as a reagent in organic synthesis, particularly in the formation of thioesters or in the introduction of sulfur-containing functionalities into organic molecules. Additionally, the compound's properties, such as solubility and stability, may be influenced by the bulky tert-butyl group, which can affect its interactions with other chemical species. Safety and handling precautions should be observed due to the potential reactivity of the chlorothionoformate functional group.

3-tert-butylphenyl chlorothionoformate

97986-06-6: 3-tert-Butylphenyl chlorothionoformate is an organic compound characterized by its functional groups and structural features. It contains a phenyl ring substituted with a tert-butyl group at the meta position, which contributes to its steric bulk and hydrophobic properties. The chlorothionoformate moiety indicates the presence of a thiocarbonyl group, where a chlorine atom is bonded to a carbon atom that is also double-bonded to sulfur. This structure suggests that the compound may exhibit reactivity typical of thioesters, including potential nucleophilic attack at the carbonyl carbon. The presence of the chlorothionoformate group can also imply that it may be used as a reagent in organic synthesis, particularly in the formation of thioesters or in the introduction of sulfur-containing functionalities into organic molecules. Additionally, the compound's properties, such as solubility and stability, may be influenced by the bulky tert-butyl group, which can affect its interactions with other chemical species. Safety and handling precautions should be observed due to the potential reactivity of the chlorothionoformate functional group.

O-(3-(tert-Butyl)phenyl) carbonochloridothioate

CAS 97986-06-6

3-tert-butylphenyl chlorothionoformate

O-(3-(tert-Butyl)phenyl) carbonochloridothioate

Ref: 54-OR1058958