CAS 1502422-51-6

spiro[3.3]heptan-2-ol

Description:

Spiro[3.3]heptan-2-ol 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 hydroxyl (-OH) group at the second carbon position, contributing to its classification as an alcohol. The spiro configuration imparts distinctive stereochemical properties, leading to potential chirality depending on the substituents attached to the rings. The compound is typically colorless and may exhibit a pleasant odor, common to many cyclic alcohols. Its solubility in polar solvents like water is moderate due to the presence of the hydroxyl group, while its hydrophobic regions from the carbon rings influence its behavior in non-polar solvents. Spiro[3.3]heptan-2-ol may have applications in organic synthesis and as a building block in the development of more complex molecules, particularly in medicinal chemistry and materials science. Its reactivity can be influenced by the functional groups present, making it a subject of interest for further chemical exploration.

Formula: C₇H₁₂O

Synonyms:

• spiro[3.3]heptan-2-ol

Spiro[3.3]heptan-2-ol

CAS: 1502422-51-6

Formula: C₇H₁₂O

Purity: 97%

Color and Shape: Liquid

Molecular weight: 112.1696

Ref: IN-DA001MF2

Spiro[3.3]heptan-2-ol

CAS: 1502422-51-6

Spiro[3.3]heptan-2-ol

Purity: ≥95%

Color and Shape: Solid

Molecular weight: 112.17g/mol

Ref: 54-OR304421

spiro[3.3]heptan-2-ol

CAS: 1502422-51-6

Formula: C₇H₁₂O

Purity: 97%

Color and Shape: Liquid, No data available.

Molecular weight: 112.172

Ref: 10-F516939

Spiro[3.3]heptan-2-ol

CAS: 1502422-51-6

Spiro[3.3]heptan-2-ol is a small molecule that has been used as a precursor in the synthesis of naphthalene derivatives. It can be obtained by the sequential elimination of two hydrogen atoms from naphthalene through oxidative cleavage. The catalytic oxidation of spiro[3.3]heptan-2-ol with molecular oxygen is an efficient and environmentally friendly method for the oxidative cleavage of benzyl alcohols to yield benzaldehydes and ketones. Spiro[3.3]heptan-2-ol can also be used as a biomolecule that binds to metal ions, such as nickel, which provides an opportunity for applications in catalysis and bioanalytical methods.

Formula: C₇H₁₂O

Purity: Min. 95%

Molecular weight: 112.17 g/mol

Ref: 3D-CKC42251