2-Acetyl-1-naphthol, 98+%
2-Acetyl-1-naphthol, 98+%
2-Acetyl-1-naphthol, 98+%
2-Acetyl-1-naphthol, 98+%
Thermo Scientific Chemicals

2-Acetyl-1-naphthol, 98+%

CAS: 711-79-5 | C12H10O2 | 186.21 g/mol
Have Questions?
Change viewbuttonViewtableView
Quantity:
25 g
100 g
Catalog number A19532.22
also known as A19532-22
Price (USD)
137.65
Special offer
Online exclusive
Ends: 30-Jun-2026
162.00
Save 24.35 (15%)
Each
Add to cart
Quantity:
100 g
Request bulk or custom format
Price (USD)
137.65
Special offer
Online exclusive
Ends: 30-Jun-2026
162.00
Save 24.35 (15%)
Each
Add to cart
Chemical Identifiers
CAS711-79-5
IUPAC Name1-(1-hydroxynaphthalen-2-yl)ethan-1-one
Molecular FormulaC12H10O2
InChI KeyJBGJVMVWYWUVOW-UHFFFAOYSA-N
SMILESCC(=O)C1=CC=C2C=CC=CC2=C1O
View more
SpecificationsSpecification SheetSpecification Sheet
Identification (FTIR)Conforms
Melting Point (clear melt)95.0-102.0°C
FormCrystals or powder or crystalline powder
Appearance (Color)Yellow
Assay (GC)≥98.0%
2-acetyl-1-naphthol and 1-acetyl-2-naphthol with triphosgene gave naphtho[1,2-e]-1,3-oxazines, naphtho[2,1-e]-1,3-oxazines or their spiro dimers depending on the molar ratio of triphosgene used for the cyclization.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
2-acetyl-1-naphthol and 1-acetyl-2-naphthol with triphosgene gave naphtho[1,2-e]-1,3-oxazines, naphtho[2,1-e]-1,3-oxazines or their spiro dimers depending on the molar ratio of triphosgene used for the cyclization.

Solubility
Insoluble in water.

Notes
Store away from strong oxidizing agents. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
RUO – Research Use Only

General References:

  1. Hossein Naeimi.; Leila Moradi. Efficient and mild synthesis of ortho-hydroxyaryl ketones catalyzed by zinc chloride under solvent-free condition and microwave irradiation. Catalysis Communications. 2006, 7, (12), 1067-1071
  2. Jessica L. Boyer.; Jodie E. Krum.; Michael C. Myers.; Aleem N. Fazal.; Carl T. Wigal. Synthetic Utility and Mechanistic Implications of the Fries Rearrangement of Hydroquinone Diesters in Boron Trifluoride Complexes. J. Org. Chem. 2000, 65, (15), 4712-4714