ETHYL 6-HYDROXY-2-NAPHTHOATE
- Product Name
- ETHYL 6-HYDROXY-2-NAPHTHOATE
- CAS No.
- 17295-12-4
- Chemical Name
- ETHYL 6-HYDROXY-2-NAPHTHOATE
- Synonyms
- Naproxen Impurity 51;Ethyl6-hydroxy-2-naphtoate;ETHYL 6-HYDROXY-2-NAPHTHOATE;ethyl 6-hydroxynaphthalene-2-carboxylate;2-Naphthalenecarboxylic acid, 6-hydroxy-, ethyl ester
- CBNumber
- CB5501764
- Molecular Formula
- C13H12O3
- Formula Weight
- 216.23
- MOL File
- 17295-12-4.mol
ETHYL 6-HYDROXY-2-NAPHTHOATE Property
- Melting point:
- 139-140.5 °C(Solv: ethanol (64-17-5))
- Boiling point:
- 378.7±15.0 °C(Predicted)
- Density
- 1.225±0.06 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,Room Temperature
- pka
- 8.83±0.40(Predicted)
- Appearance
- Light brown to brown Solid
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- 8922AA
- Product name
- Ethyl6-hydroxy-2-naphthoate
- Packaging
- 1g
- Price
- $138
- Updated
- 2021/12/16
- Product number
- 083671
- Product name
- Ethyl 6-hydroxy-2-naphthoate
- Purity
- 97%
- Packaging
- 1g
- Price
- $360
- Updated
- 2021/12/16
- Product number
- CHM0166310
- Product name
- ETHYL-6-HYDROXY-2-NAPHTHOATE
- Purity
- 98.00%
- Packaging
- 5MG
- Price
- $501.57
- Updated
- 2021/12/16
- Product number
- 17295124
- Product name
- Ethyl6-naphthol-2-carboxylate
- Packaging
- 500mg
- Price
- $1019.2
- Updated
- 2021/12/16
- Product number
- 17295124
- Product name
- Ethyl6-naphthol-2-carboxylate
- Packaging
- 1g
- Price
- $1685
- Updated
- 2021/12/16
ETHYL 6-HYDROXY-2-NAPHTHOATE Chemical Properties,Usage,Production
Synthesis
64-17-5
16712-64-4
17295-12-4
1. 6-Hydroxy-2-naphthalenecarboxylic acid (5.29 g, 28.0 mmol) was dissolved in ethanol (50 mL) at 0 °C, and thionyl chloride (6 mL) was added slowly. 2. The reaction mixture was stirred at room temperature for 72 h. 3. Upon completion of the reaction, the excess reagent was removed by rotary evaporation. 4. The residue was dissolved in ethyl acetate (100 mL), and washed with water (80 mL), cold 1M sodium bicarbonate solution (80 mL) and brine (80 mL). 5. (The residue was dissolved in ethyl acetate (100 mL) and washed sequentially with water (80 mL), cold 1 M sodium bicarbonate solution (80 mL) and brine (80 mL). 5. The organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated to give ethyl 6-hydroxy-2-naphthoate in 99% yield. 6. The product was characterized by 1H NMR (CDCl3) and LCMS (APCl): 1H NMR (CDCl3): δ 8.53 (1H, br s), 8.5 (1H, br s), 8.3 (1H, br s), 8.4 (1H, br s). , br s), 8.01 (1H, dd, J = 8.5,1.7 Hz), 7.86 (1H, d, J = 8.5 Hz), 7.20-7.13 (2H, m), 4.43 (2H, q, J = 7.3 Hz), 1.43 (3H, t, J = 7.1 Hz). lcmS (apcl): 217.1 (m + h + ).
References
[1] Patent: WO2006/40646, 2006, A1. Location in patent: Page/Page column 97
[2] Journal of Physical Chemistry A, 2016, vol. 120, # 33, p. 6563 - 6574
[3] Journal of Medicinal Chemistry, 2004, vol. 47, # 14, p. 3518 - 3536
[4] Molecular Crystals and Liquid Crystals, 2008, vol. 494, p. 282 - 292
[5] Tetrahedron, 2013, vol. 69, # 43, p. 9045 - 9055
ETHYL 6-HYDROXY-2-NAPHTHOATE Preparation Products And Raw materials
Raw materials
Preparation Products
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