CAS 15811-21-9

Spiro[2.5]octan-6-one

Description:

Spiro[2.5]octan-6-one is a bicyclic organic compound characterized by its unique spiro structure, which consists of two fused rings sharing a single carbon atom. This compound features a ketone functional group at the 6-position, contributing to its reactivity and potential applications in organic synthesis. The molecular formula typically reflects a moderate level of complexity, with a specific arrangement of carbon and hydrogen atoms that defines its physical and chemical properties. Spiro[2.5]octan-6-one is generally a colorless to pale yellow liquid or solid, depending on the temperature and purity, and it may exhibit a distinctive odor. Its chemical behavior is influenced by the presence of the carbonyl group, making it susceptible to nucleophilic attack and enabling various reactions such as condensation and cyclization. This compound has garnered interest in the fields of medicinal chemistry and materials science due to its structural features, which can be leveraged in the design of novel compounds with potential biological activity or functional properties.

Formula: C₈H₁₂O

Spiro[2.5]octan-6-one

CAS: 15811-21-9

Formula: C₈H₁₂O

Purity: 98%

Color and Shape: Liquid

Molecular weight: 124.1803

Ref: IN-DA001PZG

Spiro[2.5]octan-6-one

CAS: 15811-21-9

Spiro[2.5]octan-6-one

Purity: 97%

Ref: 54-OR1039653

Spiro[2.5]octan-6-one

CAS: 15811-21-9

Formula: C₈H₁₂O

Purity: 97%

Color and Shape: Liquid

Molecular weight: 124.183

Ref: 10-F240013

Spiro[2.5]octan-6-one

Controlled Product

CAS: 15811-21-9

Formula: C₈H₁₂O

Color and Shape: Neat

Molecular weight: 124.18

Ref: TR-S699595

Spiro[2.5]octan-6-one

CAS: 15811-21-9

Spiro[2.5]octan-6-one is a cyclopropanated biphenylene that reacts with diazomethane to form the chloride, resulting in an electron-rich spiro compound. The chloride is converted to the corresponding electron-deficient biphenylene by treatment with lead tetraacetate and cyclopropanes. The resulting biphenylenes can be reacted with an excess of cyclohexane in the presence of a catalytic amount of oriented Ni(0) to form the vinylcyclopropanes. This reaction can be used for the synthesis of dimers by reacting two vinylcyclopropanes together.

Formula: C₈H₁₂O

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 124.18 g/mol

Ref: 3D-QAA81121