1-Hydroxy-2-naphthoic acid
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1-Hydroxy-2-naphthoic acid ??
- ???
- 195-200 °C (dec.) (lit.)
- ?? ?
- 283.17°C (rough estimate)
- ??
- 1.2100 (rough estimate)
- ???
- 1.6310 (estimate)
- ???
- 150 °C
- ?? ??
- Sealed in dry,Room Temperature
- ???
- ???: ???? ???
- ??? ??
- ?? ?? ??
- ?? ?? (pKa)
- 3.02±0.30(Predicted)
- ??
- ???? ?? ???, ?????
- ???
- ??? ?? ???
- Merck
- 14,4834
- BRN
- 974438
- InChI
- 1S/C11H8O3/c12-10-8-4-2-1-3-7(8)5-6-9(10)11(13)14/h1-6,12H,(H,13,14)
- InChIKey
- SJJCQDRGABAVBB-UHFFFAOYSA-N
- SMILES
- OC(=O)c1ccc2ccccc2c1O
- LogP
- 3.196 (est)
- CAS ??????
- 86-48-6(CAS DataBase Reference)
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- ?? ? ?? ??
- ?? ? ???? ?? (GHS)
| ??? ?? | Xi | ||
|---|---|---|---|
| ?? ???? ?? | 36/37/38 | ||
| ????? | 26-36-37/39-37 | ||
| WGK ?? | 3 | ||
| TSCA | TSCA listed | ||
| HS ?? | 29182910 | ||
| ???? ??? | 11 - Combustible Solids | ||
| Hazard Classifications | Eye Irrit. 2 Skin Irrit. 2 STOT SE 3 |
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| ???? ?? | 2014-3-5763 |
1-Hydroxy-2-naphthoic acid C??? ??, ??, ??
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beige to brown-grey powder. 1-Hydroxy-2-naphthoic acid [86-48-6], C11H8O3, Mr 188.17, mp 200℃, is only sparingly soluble in hot water but readily soluble in alkali and ethanol. It couples with diazo compounds in the 4-position and, with excess, in the 4,7-positions. It is sulfonated by oleum to give the 4-sulfonic and then the 4,7-disulfonic acids. Halogenation occurs in the 4-position, and nitrosation gives 2-nitroso-1-naphthol.??
Metabolite from phenanthrene degradation. 1-Hydroxy-2-naphthoic acid is used as an intermediate for azo and triphenylmethane dyes and, more recently, for color-film dyes.?? ??
1-Hydroxy-2-naphthoic acid is produced by the transformation of phenanthrene by NCIB 9816 clones.Purification Methods
Successively crystallise the acid from EtOH/water, diethyl ether and acetonitrile, with filtration through a column of charcoal and Celite. [Tong & Glesmann J Am Chem Soc 79 583 1957, Beilstein 10 H 331, 10 IV 1194.]1-Hydroxy-2-naphthoic acid ?? ?? ? ???
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1-Hydroxy-2-naphthoic acid ?? ??
???( 436)?? ??
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