CAS 63013-56-9

Phenol, 4-tricyclo[3.3.1.13,7]dec-1-yl-, 1-acetate

Description:

Phenol, 4-tricyclo[3.3.1.1^3,7]dec-1-yl-, 1-acetate, with the CAS number 63013-56-9, is an organic compound characterized by its phenolic structure and acetate functional group. This compound features a tricyclic framework, which contributes to its unique physical and chemical properties. Typically, phenolic compounds exhibit moderate to high solubility in organic solvents and limited solubility in water due to their hydrophobic characteristics. The presence of the acetate group can enhance its reactivity, making it a potential candidate for various chemical reactions, including esterification and nucleophilic substitution. Additionally, phenolic compounds are known for their antioxidant properties, which may impart biological significance. The structural complexity of this compound may also influence its stability and reactivity under different conditions. Overall, the characteristics of this substance make it of interest in both synthetic organic chemistry and potential applications in materials science or pharmaceuticals.

Formula: C₁₈H₂₂O₂

InChI: InChI=1/C18H22O2/c1-12(19)20-17-4-2-16(3-5-17)18-9-13-6-14(10-18)8-15(7-13)11-18/h2-5,13-15H,6-11H2,1H3

InChI key: InChIKey=ARCROJYJJMBGNU-UHFFFAOYSA-N

SMILES: O(C(C)=O)C1=CC=C(C23CC4CC(C2)CC(C3)C4)C=C1

Synonyms:

• 1-(p-Acetoxyphenyl)adamantane
• 4-(1-Adamantyl)phenyl acetate
• 4-(Adamantan-1-yl)phenyl acetate
• NSC 111652
• Phenol, 4-Tricyclo[3.3.1.1~3,7~]Dec-1-Yl-, Acetate
• Phenol, 4-tricyclo[3.3.1.1^3,7]dec-1-yl-, 1-acetate
• Phenol, 4-tricyclo[3.3.1.1^3,7]dec-1-yl-, acetate
• Phenol, 4-tricyclo[3.3.1.13,7]dec-1-yl-, acetate
• Phenol, 4-tricyclo[3.3.1.13,7]dec-1-yl-, 1-acetate
• Elacestrant Impurity 3