Spiro[2.5]octan-4-one, with the CAS number 2205-98-3, is a bicyclic organic compound characterized by its unique spiro structure, which consists of two fused rings sharing a single atom. This compound features a ketone functional group at the 4-position, contributing to its reactivity and potential applications in organic synthesis. The molecular structure of spiro[2.5]octan-4-one includes a total of eight carbon atoms and a single oxygen atom, leading to a specific arrangement that influences its physical and chemical properties. Typically, spiro compounds exhibit interesting stereochemistry and can display unique conformational behavior due to the constraints of their ring systems. This compound may be of interest in various fields, including medicinal chemistry and materials science, due to its potential as a building block for more complex molecules. Its reactivity can be influenced by the presence of the ketone group, allowing for various chemical transformations. Overall, spiro[2.5]octan-4-one represents a fascinating example of spirocyclic chemistry with diverse implications in synthetic applications.

Spiro[2.5]octan-4-one

2205-98-3: Spiro[2.5]octan-4-one, with the CAS number 2205-98-3, is a bicyclic organic compound characterized by its unique spiro structure, which consists of two fused rings sharing a single atom. This compound features a ketone functional group at the 4-position, contributing to its reactivity and potential applications in organic synthesis. The molecular structure of spiro[2.5]octan-4-one includes a total of eight carbon atoms and a single oxygen atom, leading to a specific arrangement that influences its physical and chemical properties. Typically, spiro compounds exhibit interesting stereochemistry and can display unique conformational behavior due to the constraints of their ring systems. This compound may be of interest in various fields, including medicinal chemistry and materials science, due to its potential as a building block for more complex molecules. Its reactivity can be influenced by the presence of the ketone group, allowing for various chemical transformations. Overall, spiro[2.5]octan-4-one represents a fascinating example of spirocyclic chemistry with diverse implications in synthetic applications.

Spiro[2.5]octan-4-one is a three-membered ring that has absorptions in the range of 230 nm to 400 nm in the ultraviolet spectrum. It has an electronic spectrum with transitions at 12,770 cm and 13,620 cm. This compound has carbonyl groups and ketones as part of its structure. Spiro[2.5]octan-4-one absorbs at about 240 nm in the ultraviolet spectrum, which is due to its aliphatic nature.

CAS 2205-98-3

Spiro[2.5]octan-4-one

Spiro[2.5]octan-4-one

Ref: 54-OR1068206

Spiro[2.5]octan-4-one

Ref: 3D-CAA20598