CAS 23786-93-8

1,1-Diethoxycyclopentane

Description:

1,1-Diethoxycyclopentane is an organic compound characterized by its cyclopentane ring substituted with two ethoxy groups at the 1-position. This compound typically appears as a colorless liquid with a distinctive odor. Its molecular structure contributes to its relatively low polarity, making it less soluble in water but more soluble in organic solvents. The presence of the ethoxy groups enhances its reactivity, allowing it to participate in various chemical reactions, such as nucleophilic substitutions and condensation reactions. The compound's boiling point and melting point are influenced by the steric hindrance introduced by the ethoxy groups, which can affect its physical properties. Additionally, 1,1-Diethoxycyclopentane can be used as a solvent or reagent in organic synthesis, particularly in the preparation of more complex molecules. Safety considerations should be taken into account when handling this compound, as it may pose health risks if inhaled or ingested. Overall, 1,1-Diethoxycyclopentane is a versatile compound with applications in both academic research and industrial processes.

Formula: C₉H₁₈O₂

InChI: InChI=1S/C9H18O2/c1-3-10-9(11-4-2)7-5-6-8-9/h3-8H2,1-2H3

InChI key: InChIKey=QJKUIUCQENFWSS-UHFFFAOYSA-N

SMILES: O(CC)C1(OCC)CCCC1

Synonyms:

• 1,1-Diethoxycyclopentane
• Cyclopentanone diethyl ketal
• Cyclopentane, 1,1-diethoxy-
• Cyclopentanone, diethyl acetal

1,1-Diethoxycyclopentane

Controlled Product

CAS: 23786-93-8

Applications 1,1-Diethoxycyclopentane is a reagent that is used in the synthesis of Quinbolone (Q670150), which is a cyclopentenyl ether derivative of Boldenone (B675100) and also its active metabolite. Quinbolone shows weak androgenic activity.
References Balestreri, R. et al.: Arch. Maragl. Patol. Clin., 22, 369 (1966); Galletti, F. et al.: Steroids, 18, 39 (1971);

Formula: C₉H₁₈O₂

Color and Shape: Neat

Molecular weight: 158.24

Ref: TR-D441975