For research use only. Not for therapeutic Use.
Ethyl 2-naphthoate (Cat No.:I014371) is an organic compound belonging to the ester class. It is derived from naphthalene and contains an ethyl ester group (-COOCH2CH3) attached to a naphthalene ring. Ethyl 2-naphthoate finds applications in various industries. It is commonly used as a fragrance ingredient in perfumes, soaps, and personal care products due to its pleasant aromatic properties. Additionally, it serves as a flavoring agent in the food and beverage industry, providing a distinctive flavor to certain products.
| Catalog Number | I014371 |
| CAS Number | 3007-91-8 |
| Synonyms | Ethyl 2-naphthoate; AI3-11104; AI3 11104; AI311104;2-Naphthalenecarboxylic acid, ethyl ester |
| Molecular Formula | C13H12O2 |
| Purity | ≥95% |
| Solubility | Soluble in DMSO |
| IUPAC Name | ethyl naphthalene-2-carboxylate |
| InChI | InChI=1S/C13H12O2/c1-2-15-13(14)12-8-7-10-5-3-4-6-11(10)9-12/h3-9H,2H2,1H3 |
| InChIKey | HQKSINSCHCDMLS-UHFFFAOYSA-N |
| SMILES | CCOC(=O)C1=CC2=CC=CC=C2C=C1 |
| Reference | </br> 1: Park C, Lee PH. Indium-mediated regio- and chemoselective synthesis of alpha-hydroxyalkyl allenic esters and gold-catalyzed cyclizations to ethyl 2-naphthoate derivatives. Org Lett. 2008 Aug 7;10(15):3359-62. doi: 10.1021/ol801196g. Epub 2008 Jul 10. PubMed PMID: 18613690.</br>2: Narayana B, Vijaya Raj KK, Ashalatha BV, Kumari NS. Synthesis of some new 2-(6-methoxy-2-naphthyl)- 5-aryl-1,3,4-oxadiazoles as possible non-steroidal anti-inflammatory and analgesic agents. Arch Pharm (Weinheim). 2005 Aug;338(8):373-7. PubMed PMID: 16041838.</br>3: Carr DO, Metzler DE. The oxidation of ethyl 1,2-dihydro-2-naphthoate by flavins and its stimulation by light. Biochim Biophys Acta. 1970 Apr 7;205(1):63-71. PubMed PMID: 5439518.</br></br> |
