Acetic acid, [(1-benzoyl-2-naphthalenyl)oxy]-, ethyl ester

Base Information

Chemical Name:Acetic acid, [(1-benzoyl-2-naphthalenyl)oxy]-, ethyl ester
CAS No.:94866-93-0
Molecular Formula:C21H18O4
Molecular Weight:334.372
Hs Code.:
DSSTox Substance ID:DTXSID90479766
Wikidata:Q82313981

Synonyms:Acetic acid, [(1-benzoyl-2-naphthalenyl)oxy]-, ethyl ester;94866-93-0;DTXSID90479766

Suppliers and Price of Acetic acid, [(1-benzoyl-2-naphthalenyl)oxy]-, ethyl ester

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

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Chemical Property of Acetic acid, [(1-benzoyl-2-naphthalenyl)oxy]-, ethyl ester

Chemical Property:

XLogP3:4.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:7
Exact Mass:334.12050905
Heavy Atom Count:25
Complexity:455

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC(=O)COC1=C(C2=CC=CC=C2C=C1)C(=O)C3=CC=CC=C3

Technology Process of Acetic acid, [(1-benzoyl-2-naphthalenyl)oxy]-, ethyl ester

There total 3 articles about Acetic acid, [(1-benzoyl-2-naphthalenyl)oxy]-, ethyl ester 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: 98.0%

: 6333-07-9
1-benzoyl-2-naphthol

: 105-36-2
ethyl bromoacetate

: 94866-93-0
<1-Benzoyl-naphthyl-(2)-oxy>-essigsaeure-aethylester

Guidance literature:: With potassium carbonate; In acetone; for 2h; Heating;
DOI:10.1016/j.tet.2004.11.022

Reference yield:

: 93-04-9
2-Methoxynaphthalene

: 94866-93-0
<1-Benzoyl-naphthyl-(2)-oxy>-essigsaeure-aethylester

Guidance literature:: Multi-step reaction with 2 steps

1: AlCl₃ / CH₂Cl₂ / 18 h / 20 °C

2: K₂CO₃ / acetone / Heating

With aluminium trichloride; potassium carbonate; In dichloromethane; acetone;
DOI:10.1016/j.bmcl.2005.10.105

Reference yield:

: 98-88-4
benzoyl chloride

: 94866-93-0
<1-Benzoyl-naphthyl-(2)-oxy>-essigsaeure-aethylester

Guidance literature:: Multi-step reaction with 2 steps

1: AlCl₃ / CH₂Cl₂ / 18 h / 20 °C

2: K₂CO₃ / acetone / Heating

With aluminium trichloride; potassium carbonate; In dichloromethane; acetone;
DOI:10.1016/j.bmcl.2005.10.105