7-Phenoxy-1,2,3,4-tetrahydronaphthalen-1-one

Base Information

Chemical Name:7-Phenoxy-1,2,3,4-tetrahydronaphthalen-1-one
CAS No.:151453-21-3
Molecular Formula:C₁₆H₁₄O₂
Molecular Weight:238.286
Hs Code.:
European Community (EC) Number:621-128-9

Synonyms:7-phenoxy-1,2,3,4-tetrahydronaphthalen-1-one;151453-21-3;7-phenoxy-3,4-dihydro-2H-naphthalen-1-one;7-phenoxy-3,4-dihydronaphthalen-1(2h)-one;7-PHENOXY-1-TETRALONE;SCHEMBL7590260;ZFOLQUQHELUVNU-UHFFFAOYSA-N;AKOS012023514;EN300-191142

Suppliers and Price of 7-Phenoxy-1,2,3,4-tetrahydronaphthalen-1-one

Supply Marketing:

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

Manufacturers and distributors:

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Total 1 raw suppliers

Chemical Property of 7-Phenoxy-1,2,3,4-tetrahydronaphthalen-1-one

Chemical Property:

XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:238.099379685
Heavy Atom Count:18
Complexity:294

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CC2=C(C=C(C=C2)OC3=CC=CC=C3)C(=O)C1

Technology Process of 7-Phenoxy-1,2,3,4-tetrahydronaphthalen-1-one

There total 4 articles about 7-Phenoxy-1,2,3,4-tetrahydronaphthalen-1-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: 25.0%

: 6958-94-7
4-(4-phenoxyphenyl)butyric acid

: 151453-21-3
7-phenoxy-3,4-dihydro-2H-naphthalen-1-one

Guidance literature:: With PPA; at 110 ℃; for 12h;

Reference yield:

: 108-86-1,52753-63-6
bromobenzene

copper(II) oxide: copper(II) oxide

: 22009-38-7
7-hydroxy-1-tetralone

: 151453-21-3
7-phenoxy-3,4-dihydro-2H-naphthalen-1-one

Guidance literature:: With potassium carbonate; In pyridine; hexane; ethyl acetate;

Reference yield:

: 101-84-8
diphenylether

: 151453-21-3
7-phenoxy-3,4-dihydro-2H-naphthalen-1-one

Guidance literature:: Multi-step reaction with 3 steps

1: 90 percent / AlCl₃ / benzene / 3 h / Heating

2: 80 percent / KOH, aq. hydrazine hydrate / bis-(2-hydroxy-ethyl) ether / a) reflux, 1 h, b) 200 deg C, 4 h

3: 25 percent / polyphosphoric acid / 12 h / 110 °C

With potassium hydroxide; aluminium trichloride; PPA; hydrazine hydrate; In diethylene glycol; benzene;