structure of 2-iso-Propoxyphenethyl alcohol

2-iso-Propoxyphenethyl alcohol

CAS No.: 1000505-33-8
M. Wt: 180.24
M. Fa: C11H16O2
InChI Key: ICSGTKCQDRPWBD-UHFFFAOYSA-N

Names and Identifiers of 2-iso-Propoxyphenethyl alcohol

CAS Number

1000505-33-8

MDL Number

MFCD09926383

IUPAC Name

2-(2-propan-2-yloxyphenyl)ethanol

InChI

InChI=1S/C11H16O2/c1-9(2)13-11-6-4-3-5-10(11)7-8-12/h3-6,9,12H,7-8H2,1-2H3

InChIKey

ICSGTKCQDRPWBD-UHFFFAOYSA-N

Canonical SMILES

CC(C)OC1=CC=CC=C1CCO

UNSPSC Code

12352100

Physical and chemical properties of 2-iso-Propoxyphenethyl alcohol

Molecular Formula

C11H16O2

Molecular Weight

180.24

Safety Information of 2-iso-Propoxyphenethyl alcohol

Pictograms

Signal Word

Warning

Safety Data Sheet

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

Applications of 2-iso-Propoxyphenethyl alcohol

2-(2-Isopropoxyphenyl)ethanol finds applications across various fields:

  • Pharmaceutical Industry: It serves as an intermediate in the synthesis of pharmaceutical compounds due to its structural properties and biological activity.
  • Chemical Manufacturing: Used as a solvent and reagent in organic synthesis, it facilitates reactions involving other compounds.
  • Cosmetics and Personal Care Products: Its properties make it suitable for use in formulations where skin penetration and moisture retention are desired.
  • Research

Interaction Studies of 2-iso-Propoxyphenethyl alcohol

Studies on 2-(2-Isopropoxyphenyl)ethanol's interactions focus on its ability to modulate enzyme activity and receptor signaling pathways. The hydroxyl group allows for hydrogen bonding with biological macromolecules, potentially influencing metabolic processes. Research continues into its efficacy as an antimicrobial agent, exploring how structural variations affect its activity against different pathogens.

Biological Activity of 2-iso-Propoxyphenethyl alcohol

Research indicates that 2-(2-Isopropoxyphenyl)ethanol may exhibit biological activities, particularly in antimicrobial and antioxidant domains. The presence of the hydroxyl group enhances its potential to act as a hydrogen donor, which may contribute to its antioxidant properties. Additionally, studies suggest that compounds with similar structures can interact with biological targets, leading to various pharmacological effects.