5-Chloro-2-adamantanone is an organic compound characterized by its adamantane structure, which is a polycyclic hydrocarbon known for its stability and rigidity. This compound features a ketone functional group and a chlorine atom substituted at the 5-position of the adamantane framework. It typically appears as a solid at room temperature and is soluble in organic solvents. The presence of the chlorine atom introduces unique reactivity and properties, making it of interest in various chemical syntheses and applications. The compound is often utilized in medicinal chemistry and material science due to its potential biological activity and structural properties. Its molecular formula reflects the presence of carbon, hydrogen, and chlorine, contributing to its overall chemical behavior. Safety data should be consulted for handling, as with many organic compounds, to ensure proper precautions are taken. Overall, 5-Chloro-2-adamantanone exemplifies the intersection of structural complexity and functional versatility in organic chemistry.

5-Chloro-2-adamantanone

20098-17-3: 5-Chlorotricyclo[3.3.1.1~3,7~]Decan-2-One

5-Chloroadamantan-2-one

5-Chloro-1-adamantanone

5-Chloro-2-adamantanone is an organic solvent that has nucleophilic properties. It can act as a reactive, nucleophile, or carbonyl group. 5-Chloro-2-adamantanone is synthesized by the reaction of 2-chloroadamantane with chlorosulfonic acid in the presence of zinc chloride at room temperature. The yield of this reaction is dependent on the concentration of zinc chloride used and ranges from 23% to 66%. This reaction can be optimized by altering the reaction time and temperature, as well as by using different halides.

CAS 20098-17-3: 5-Chloro-2-adamantanone

5-Chloroadamantan-2-one

Ref: 10-F324785

5-Chloro-2-adamantanone

Ref: 3B-C2140

5-Chloroadamantan-2-one

Ref: 54-OR95903

5-Chloro-1-adamantanone

Ref: 7W-GK8954

5-Chloro-2-adamantanone

Ref: 3D-FC07726

Tricyclo[3.3.1.13,7]decan-2-one, 5-chloro-

Ref: IN-DA002D4G