Isochroman-6-ol
CAS No.:
412338-41-1
M. Wt:
150.174
M. Fa:
C9H10O2
InChI Key:
YXPMZDNYHFWZJI-UHFFFAOYSA-N
Appearance:
White Solid
Names and Identifiers of Isochroman-6-ol
CAS Number |
412338-41-1 |
|---|---|
EC Number |
870-478-0 |
MDL Number |
MFCD18416390 |
IUPAC Name |
3,4-dihydro-1H-isochromen-6-ol |
InChI |
InChI=1S/C9H10O2/c10-9-2-1-8-6-11-4-3-7(8)5-9/h1-2,5,10H,3-4,6H2 |
InChIKey |
YXPMZDNYHFWZJI-UHFFFAOYSA-N |
Canonical SMILES |
C1COCC2=C1C=C(C=C2)O |
UNSPSC Code |
12352100 |
Physical and chemical properties of Isochroman-6-ol
Boiling Point |
311.6±42.0 °C at 760 mmHg |
|---|---|
Density |
1.2±0.1 g/cm3 |
Exact Mass |
150.068085 |
Flash Point |
153.5±22.1 °C |
H Bond Acceptors |
2 |
H Bond Donors |
1 |
Index of Refraction |
1.581 |
LogP |
1.32 |
Molecular Formula |
C9H10O2 |
Molecular Weight |
150.174 |
Vapour Pressure |
0.0±0.7 mmHg at 25°C |
Safety Information of Isochroman-6-ol
Applications of Isochroman-6-ol
Isochroman-6-ol has several notable applications:
- Pharmaceuticals: Its derivatives are being explored for their potential therapeutic effects, including anti-inflammatory and neuroprotective activities.
- Organic Synthesis: Isochroman structures serve as intermediates in the synthesis of more complex organic molecules, particularly in the development of natural products and pharmaceuticals .
- Material Science: The compound's unique structural properties make it useful in developing advanced materials and polymers.
Biological Activity of Isochroman-6-ol
Research indicates that isochroman derivatives possess various biological activities. Isochroman-6-ol has been studied for its potential:
- Antioxidant Properties: Compounds within the isochroman family have shown promise in scavenging free radicals, which may contribute to their protective effects against oxidative stress .
- Antimicrobial Activity: Some studies suggest that isochromans exhibit antimicrobial properties, making them potential candidates for developing new antibiotics .
Physical sample testing spectrum (NMR) of Isochroman-6-ol
