6-Hydroxy-2-naphthaldehyde

6-Hydroxy-2-naphthaldehyde

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6-Hydroxy-2-naphthaldehyde Basic information
6-Hydroxy-2-naphthaldehyde
6-Hydroxynaphthalene-2-carboxaldehyde, 2-Formyl-6-hydroxynaph;6-Hydroxy-2-naphthaldehyde 95%;6-hydroxy-2-naphtalenecarbaldehyde;6-HYDROXY-2-NAPHTHALDEHYDE;2-Hydroxy-6-Naphthaldehyde;6-HYDROXY-2-NAPHTHALDEHYDE, 99+%;2-Naphthol-6-carboxaldehyde;6-Hydroxynaphthalene-2-carboxaldehyde, 2-Formyl-6-hydroxynaphthalene
78119-82-1
C11H8O2
172.18
 
78119-82-1.mol
6-Hydroxy-2-naphthaldehyde Structure
 
6-Hydroxy-2-naphthaldehyde Chemical Properties
178-180
373.4±15.0 degree (Predicted)
1.288±0.06 g/cm3(Predicted)
8.60±0.40(Predicted)
78119-82-1(CAS DataBase Reference)
 
52
2912490090
 
 
 
6-Hydroxy-2-naphthaldehyde Usage And Synthesis
A stirring bar, 0.35 g (2.01 mmol) of 6-hydroxy-2-naphthylcarbinol and 20 mL of N, N-dimethylformamide were introduced into a 100 mL flask to form a homogenous mixture. This mixture was added with 3.5 g (36.94 mmol) of electrolytic manganese dioxide (FMH, Tosoh, purity: 91.77 per cent) and vigorously stirred for 16 hours while the mixture was maintained at 20 degree . The reaction mixture was analyzed by using liquid chromatography. As a result, it was found that the conversion of the 6-hydroxy-2-naphthylcarbinol was 92.3 per cent, and the yield of the 6-hydroxy-2-naphthaldehyde was 87 percent.
 
6-Hydroxy-2-naphthaldehyde Preparation Products And Raw materials
2-Naphthalenecarbonitrile, 6-formyl--->6-Methoxy-2-naphthaldehyde-->6-(Hydroxymethyl)-2-naphthol-->METHYL 6-HYDROXY-2-NAPHTHOATE-->4-Hydroxy-2,2,6,6-tetramethyl-piperidinooxy

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