Acetonitrile, [(1-benzoyl-2-naphthalenyl)oxy]-

Base Information

Chemical Name:Acetonitrile, [(1-benzoyl-2-naphthalenyl)oxy]-
CAS No.:833485-63-5
Molecular Formula:C19H13NO2
Molecular Weight:287.318
Hs Code.:
DSSTox Substance ID:DTXSID10479768

Synonyms:833485-63-5;Acetonitrile, [(1-benzoyl-2-naphthalenyl)oxy]-;DTXSID10479768

Suppliers and Price of Acetonitrile, [(1-benzoyl-2-naphthalenyl)oxy]-

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
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price

Total 1 raw suppliers

Chemical Property of Acetonitrile, [(1-benzoyl-2-naphthalenyl)oxy]-

Chemical Property:

XLogP3:4.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:287.094628657
Heavy Atom Count:22
Complexity:432

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)C2=C(C=CC3=CC=CC=C32)OCC#N

Technology Process of Acetonitrile, [(1-benzoyl-2-naphthalenyl)oxy]-

There total 3 articles about Acetonitrile, [(1-benzoyl-2-naphthalenyl)oxy]- 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: 99.0%

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

: 590-17-0
cyanomethyl bromide

: 833485-63-5
(1-benzoyl-naphthalen-2-yloxy)-acetonitrile

Guidance literature:: With potassium carbonate; In acetone; at 30 ℃;
DOI:10.1016/j.tet.2004.11.022

Reference yield:

: 93-04-9
2-Methoxynaphthalene

: 833485-63-5
(1-benzoyl-naphthalen-2-yloxy)-acetonitrile

Guidance literature:: Multi-step reaction with 2 steps

1.1: AlCl₃ / CH₂Cl₂ / 20 h / 20 °C

1.2: 77 percent / aq. HCl / CH₂Cl₂ / 1 h

2.1: 99 percent / K₂CO₃ / acetone / 30 °C

With aluminium trichloride; potassium carbonate; In dichloromethane; acetone;
DOI:10.1016/j.tet.2004.11.022

Reference yield:

: 98-88-4
benzoyl chloride

: 833485-63-5
(1-benzoyl-naphthalen-2-yloxy)-acetonitrile

Guidance literature:: Multi-step reaction with 2 steps

1.1: AlCl₃ / CH₂Cl₂ / 20 h / 20 °C

1.2: 77 percent / aq. HCl / CH₂Cl₂ / 1 h

2.1: 99 percent / K₂CO₃ / acetone / 30 °C

With aluminium trichloride; potassium carbonate; In dichloromethane; acetone;
DOI:10.1016/j.tet.2004.11.022