5-[(Naphthalen-1-yl)methyl]-3-phenylcyclopent-2-en-1-one

Base Information

Chemical Name:5-[(Naphthalen-1-yl)methyl]-3-phenylcyclopent-2-en-1-one
CAS No.:105850-98-4
Molecular Formula:C₂₂H₁₈O
Molecular Weight:298.384
Hs Code.:
DSSTox Substance ID:DTXSID40552614
Nikkaji Number:J986.193I

Synonyms:105850-98-4;DTXSID40552614;5-[(Naphthalen-1-yl)methyl]-3-phenylcyclopent-2-en-1-one

Suppliers and Price of 5-[(Naphthalen-1-yl)methyl]-3-phenylcyclopent-2-en-1-one

Supply Marketing:

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

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Chemical Property of 5-[(Naphthalen-1-yl)methyl]-3-phenylcyclopent-2-en-1-one

Chemical Property:

XLogP3:5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:298.135765193
Heavy Atom Count:23
Complexity:457

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(C(=O)C=C1C2=CC=CC=C2)CC3=CC=CC4=CC=CC=C43

Technology Process of 5-[(Naphthalen-1-yl)methyl]-3-phenylcyclopent-2-en-1-one

There total 7 articles about 5-[(Naphthalen-1-yl)methyl]-3-phenylcyclopent-2-en-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: 40.0%

: 111200-29-4
ethyl 2-acetyl-2-(1-naphtylmethyl)-4-oxo-4-phenylbutanoate

: 105850-98-4
5-(1-Naphthylmethyl)-3-phenylcyclopent-2-enone

Guidance literature:: With potassium hydroxide; reflux, 4 h, then reflux 4 h;

Reference yield:

: 88022-93-9
1-(ethoxycarbonyl)-1-(1-naphthylmethyl)-2-propanone

: 105850-98-4
5-(1-Naphthylmethyl)-3-phenylcyclopent-2-enone

Guidance literature:: Multi-step reaction with 2 steps

1: NaH / 1,2-dimethoxy-ethane / 10 min, then 20 deg C, 12 h

2: 40 percent / 1.) 1percent aq. KOH; 2.) 10percent aq. KOH / reflux, 4 h, then reflux 4 h

With potassium hydroxide; sodium hydride; In 1,2-dimethoxyethane;

Reference yield:

: 70-11-1
α-bromoacetophenone

: 105850-98-4
5-(1-Naphthylmethyl)-3-phenylcyclopent-2-enone

Guidance literature:: Multi-step reaction with 2 steps

1: NaH / 1,2-dimethoxy-ethane / 10 min, then 20 deg C, 12 h

2: 40 percent / 1.) 1percent aq. KOH; 2.) 10percent aq. KOH / reflux, 4 h, then reflux 4 h

With potassium hydroxide; sodium hydride; In 1,2-dimethoxyethane;