structure of 2-(6-Propoxynaphthalen-1-Yl)Propane-1,3-Diol

2-(6-Propoxynaphthalen-1-Yl)Propane-1,3-Diol

CAS No.: 1000340-10-2
M. Wt: 260.33
M. Fa: C16H20O3
InChI Key: DSGHIEYBWHROTQ-UHFFFAOYSA-N

Names and Identifiers of 1000340-10-2

CAS Number

1000340-10-2

MDL Number

MFCD09910432

IUPAC Name

2-(6-propoxynaphthalen-1-yl)propane-1,3-diol

InChI

InChI=1S/C16H20O3/c1-2-8-19-14-6-7-16-12(9-14)4-3-5-15(16)13(10-17)11-18/h3-7,9,13,17-18H,2,8,10-11H2,1H3

InChIKey

DSGHIEYBWHROTQ-UHFFFAOYSA-N

Canonical SMILES

CCCOC1=CC=C2C(=C1)C=CC=C2C(CO)CO

UNSPSC Code

12352100

Physical and chemical properties of 1000340-10-2

Molecular Formula

C16H20O3

Molecular Weight

260.33

Safety Information of 1000340-10-2

Pictograms

Signal Word

 Warning

Safety Data Sheet
Supports customized editing of SDS information and downloading in PDF documents.

Applications of 1000340-10-2

2-(6-Propoxynaphthalen-1-YL)propane-1,3-diol finds applications primarily in:

  • Proteomics Research: As a reagent for studying protein interactions and modifications.
  • Chemical Synthesis: Serving as an intermediate in the synthesis of more complex organic molecules.

Its unique structure allows it to play a role in developing new materials or pharmaceuticals.

Interaction Studies of 1000340-10-2

Interaction studies involving 2-(6-Propoxynaphthalen-1-YL)propane-1,3-diol typically focus on its role as a ligand or substrate in biochemical assays. Understanding how this compound interacts with proteins or other biomolecules can provide insights into its functionality in biological systems.

Research into its binding affinities and mechanisms of action will further elucidate its potential uses in therapeutic applications or as a tool in biochemical research.

Biological Activity of 1000340-10-2

While specific biological activity data for 2-(6-Propoxynaphthalen-1-YL)propane-1,3-diol is limited, compounds with similar structures often exhibit various biological properties. For instance:

  • Antimicrobial Activity: Many diols and naphthalene derivatives are known to possess antimicrobial properties.
  • Potential Antioxidant Effects: The presence of hydroxyl groups may contribute to antioxidant activity.

Further research is necessary to elucidate the specific biological effects of this compound.