6-ethoxy-3,4-dihydronaphthalen-1(2H)-one

Base Information

• Chemical Name: 6-ethoxy-3,4-dihydronaphthalen-1(2H)-one
• CAS No.: 50676-12-5
• Molecular Formula: C12H14O2
• Molecular Weight: 190.23800
• Hs Code.: 2914509090
• DSSTox Substance ID: DTXSID80517146
• Wikidata: Q82378963
• Mol file: 50676-12-5.mol

Synonyms:6-ethoxy-3,4-dihydronaphthalen-1(2H)-one;50676-12-5;6-ethoxy-3,4-dihydro-2H-naphthalen-1-one;6-ethoxy-1,2,3,4-tetrahydronaphthalen-1-one;SCHEMBL6825249;DTXSID80517146;AM9345;AKOS011107595;J-518679

Chemical Property of 6-ethoxy-3,4-dihydronaphthalen-1(2H)-one

Chemical Property:

• PSA: 26.30000
• LogP: 2.60430
• Storage Temp.: 2-8°C
• XLogP3: 2.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 190.099379685
• Heavy Atom Count: 14
• Complexity: 212

Purity/Quality:

99%, ^*data from raw suppliers

6-Ethoxy-3,4-dihydronaphthalen-1(2H)-one 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCOC1=CC2=C(C=C1)C(=O)CCC2

Technology Process of 6-ethoxy-3,4-dihydronaphthalen-1(2H)-one

There total 4 articles about 6-ethoxy-3,4-dihydronaphthalen-1(2H)-one 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: 85.0%

ethyl bromide (74-96-4) + 6-Hydroxy-1-tetralone (3470-50-6) → ethoxynaphthalenone (50676-12-5)

Guidance literature:

With potassium carbonate; potassium iodide; In N,N-dimethyl-formamide; at 100 ℃; for 3h;

DOI:10.1248/cpb.31.2329

Reference yield:

4-(3-ethoxy-phenyl)-butyric acid → ethoxynaphthalenone (50676-12-5)

Guidance literature:

With sulfuric acid;

Reference yield:

4-(3-ethoxy-phenyl)-butyronitrile (873989-42-5) → ethoxynaphthalenone (50676-12-5)

Guidance literature:

Multi-step reaction with 2 steps

2: aqueous H₂SO₄

With sulfuric acid;

upstream raw materials:

ethyl bromide

6-Hydroxy-1-tetralone

4-(3-ethoxy-phenyl)-butyronitrile

Downstream raw materials:

C₁₉H₂₁NO₄S