N8505
1-Naphthyl acetate
≥98% (C)
Synonym(s):
α-Naphthyl acetate
About This Item
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Quality Level
Assay
≥98% (C)
form
crystals
mp
43-46 °C (lit.)
storage temp.
−20°C
SMILES string
CC(=O)Oc1cccc2ccccc12
InChI
1S/C12H10O2/c1-9(13)14-12-8-4-6-10-5-2-3-7-11(10)12/h2-8H,1H3
InChI key
VGKONPUVOVVNSU-UHFFFAOYSA-N
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General description
Application
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
235.4 °F
Flash Point(C)
113 °C
Certificates of Analysis (COA)
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Articles
The Fries rearrangement reaction is an organic name reaction which involves the conversion of phenolic esters into hydroxyaryl ketones on heating in the presence of a catalyst. Suitable catalysts for this reaction are Brønsted or Lewis acids such as HF, AlCl3, BF3, TiCl4, or SnCl4. The Fries rearrangement reaction is an ortho, para-selective reaction, and is used in the preparation of acyl phenols. This organic reaction has been named after German chemist Karl Theophil Fries.
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