structure of Propyl adamantane-1-carboxylate

Propyl adamantane-1-carboxylate

CAS No.: 24556-15-8
M. Wt: 222.323
M. Fa: C14H22O2
InChI Key: LVGMTYKQVATOOP-UHFFFAOYSA-N

Names and Identifiers of Propyl adamantane-1-carboxylate

CAS Number

24556-15-8

IUPAC Name

propyl adamantane-1-carboxylate

InChI

InChI=1S/C14H22O2/c1-2-3-16-13(15)14-7-10-4-11(8-14)6-12(5-10)9-14/h10-12H,2-9H2,1H3

InChIKey

LVGMTYKQVATOOP-UHFFFAOYSA-N

Canonical SMILES

CCCOC(=O)C12CC3CC(C1)CC(C3)C2

Physical and chemical properties of Propyl adamantane-1-carboxylate

Boiling Point

277.1±8.0 °C at 760 mmHg

Density

1.1±0.1 g/cm3

Exact Mass

222.161987

Flash Point

120.8±6.0 °C

Index of Refraction

1.521

LogP

4.12

Molecular Formula

C14H22O2

Molecular Weight

222.323

PSA

26.30000

Storage condition

2-8°C

Vapour Pressure

0.0±0.6 mmHg at 25°C

Applications of Propyl adamantane-1-carboxylate

Propyl adamantane-1-carboxylate has diverse applications across several fields:

  • Chemistry: It serves as a building block for synthesizing more complex organic molecules.
  • Biology: The compound is utilized in biological studies, particularly in drug development.
  • Medicine: Its derivatives show promise in treating various diseases, including viral infections and neurological disorders.
  • Industry: It is used in producing advanced materials such as polymers and nanomaterials due to its unique structural properties.

Interaction Studies of Propyl adamantane-1-carboxylate

The interaction studies of propyl adamantane-1-carboxylate focus on its biological mechanisms and pharmacological effects. The compound's ability to modulate biological processes through interactions with specific molecular targets makes it a subject of interest in drug discovery research. Understanding these interactions is crucial for developing effective therapeutic agents based on this compound.

Biological Activity of Propyl adamantane-1-carboxylate

Research indicates that propyl adamantane-1-carboxylate and its derivatives may exhibit significant biological activities. The compound's structure allows it to interact with various biological targets, potentially influencing enzymatic pathways and receptor interactions. Notably, derivatives of this compound have been investigated for their antiviral properties, particularly in the context of treating viral infections and neurological disorders. The adamantane moiety is known for enhancing the stability and bioavailability of pharmaceutical compounds.

Retrosynthesis analysis of Propyl adamantane-1-carboxylate

  • Route#1

    Cas:23074-42-2
    Cas:24556-15-8