3-Hydroxy-2-naphthoic acid
3-Hydroxy-2-naphthoic acid is an organic compound with the formula C10H6(OH)(CO2H). It is one of the several carboxylic acids derived from 2-naphthol. It is a common precursor to azo dyes and pigments. It is prepared by carboxylation of 2-naphthol via the Kolbe–Schmitt reaction.[1]
Names | |
---|---|
Preferred IUPAC name
3-Hydroxynaphthalene-2-carboxylic acid | |
Other names
3-Hydroxy-2-naphthoic acid BON acid β-Hydroxynaphthoic acid | |
Identifiers | |
3D model (JSmol) |
|
744100 | |
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.001.983 |
EC Number |
|
KEGG | |
PubChem CID |
|
RTECS number |
|
UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
Properties | |
C11H8O3 | |
Molar mass | 188.182 g·mol−1 |
Appearance | Yellow solid |
Melting point | 222 °C (432 °F; 495 K) |
Hazards | |
GHS labelling: | |
Warning | |
H302, H312, H317, H319, H361, H371, H412 | |
P201, P202, P260, P261, P264, P270, P272, P273, P280, P281, P301+P312, P302+P352, P305+P351+P338, P308+P313, P309+P311, P312, P321, P322, P330, P333+P313, P337+P313, P363, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references |
3-Hydroxy-2-naphthoic acid is a precursor to many anilides, such as Naphthol AS, which are reactive toward diazonium salts to give deeply colored azo compounds. Azo coupling of 3-hydroxy-2-naphthoic acid gives many dyes as well.
References
- Gerald Booth (2005). "Naphthalene Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_009..
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.