Ethyl 2-hydroxynaphthalene-1-carboxylate

Base Information

Chemical Name:Ethyl 2-hydroxynaphthalene-1-carboxylate
CAS No.:52159-66-7
Molecular Formula:C13H12O3
Molecular Weight:216.23
Hs Code.:2918290000
DSSTox Substance ID:DTXSID30568269
Nikkaji Number:J282.343H
Wikidata:Q82454468
Mol file:52159-66-7.mol

Synonyms:52159-66-7;ethyl 2-hydroxynaphthalene-1-carboxylate;Ethyl 2-hydroxy-1-naphthoate;ETHYL-2-HYDROXY-1-NAPHTHALENE CARBOXYLATE;ETHYL 2-HYDROXY-1-NAPHTHALENE CARBOXYLATE;DTXSID30568269;ETHYL-2-HYDROXY-1-NAPHTHALENECARBOXYLATE

Suppliers and Price of Ethyl 2-hydroxynaphthalene-1-carboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
ETHYL-2-HYDROXY-1-NAPHTHALENE CARBOXYLATE 95.00%
5MG
$ 500.41

Alichem
Ethyl2-naphthol-1-carboxylate
1g
$ 1735.55

Alichem
Ethyl2-naphthol-1-carboxylate
500mg
$ 980.00

Alichem
Ethyl2-naphthol-1-carboxylate
250mg
$ 714.00

Total 4 raw suppliers

Chemical Property of Ethyl 2-hydroxynaphthalene-1-carboxylate

Chemical Property:

PSA：46.53000
LogP:2.72210
XLogP3:3.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:216.078644241
Heavy Atom Count:16
Complexity:252

Purity/Quality:

99% ^*data from raw suppliers

ETHYL-2-HYDROXY-1-NAPHTHALENE CARBOXYLATE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C1=C(C=CC2=CC=CC=C21)O

Technology Process of Ethyl 2-hydroxynaphthalene-1-carboxylate

There total 7 articles about Ethyl 2-hydroxynaphthalene-1-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 88.0%

: 866251-15-2
(1H-benzo[d][1,2,3]triazol-1-yl)(2-hydroxynaphthalen-1-yl)methanone

: 64-17-5
ethanol

: 52159-66-7
ethyl 2-hydroxy-1-naphthoate

Guidance literature:: at 120 ℃; for 0.166667h; microwave irradiation;
DOI:10.1021/jo052293q

Reference yield: 65.0%

: 870673-71-5
ethyl (4Z)-2-diazo-3-oxo-5-phenylpent-4-enoate

: 52159-66-7
ethyl 2-hydroxy-1-naphthoate

Guidance literature:: With dirhodium tetraacetate; In dichloromethane; at 20 ℃; for 12h;
DOI:10.1016/j.tet.2005.05.106

Reference yield: 44.0%

: 3007-97-4
ethyl 1-naphthoate

: 18500-83-9
ethyl 8-hydroxy-1-naphthoate

: 52159-66-7
ethyl 2-hydroxy-1-naphthoate

Guidance literature:: With dipotassium peroxodisulfate; [ruthenium(II)(η⁶-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]₂; trifluoroacetic acid; trifluoroacetic anhydride; at 70 ℃; for 11h;
DOI:10.1021/ol301104n