5-Methoxynaphthalene-1,2-dione

Base Information

Chemical Name:5-Methoxynaphthalene-1,2-dione
CAS No.:61539-67-1
Molecular Formula:C₁₁H₈O₃
Molecular Weight:188.183
Hs Code.:
DSSTox Substance ID:DTXSID00491419
Nikkaji Number:J859.527E
Wikidata:Q82335973

Synonyms:5-Methoxynaphthalene-1,2-dione;61539-67-1;SCHEMBL5886287;5-methoxy-[1,2]naphthoquinone;DTXSID00491419;VVCISDXAHHGMBS-UHFFFAOYSA-N;PD147984

Suppliers and Price of 5-Methoxynaphthalene-1,2-dione

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
Packaging
price

Total 3 raw suppliers

Chemical Property of 5-Methoxynaphthalene-1,2-dione

Chemical Property:

XLogP3:1.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:188.047344113
Heavy Atom Count:14
Complexity:293

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=CC2=C1C=CC(=O)C2=O

Technology Process of 5-Methoxynaphthalene-1,2-dione

There total 1 articles about 5-Methoxynaphthalene-1,2-dione 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:

: 3588-80-5
5-methoxynaphthalen-1-ol

: 61539-67-1
5-methoxy[1,2]naphthoquinone

: 4923-61-9
5-methoxynaphthoquinone

Guidance literature:: With salcomine; oxygen; In acetonitrile; for 2h; Yield given. Yields of byproduct given; Ambient temperature;

Reference yield:

: 61539-67-1
5-methoxy[1,2]naphthoquinone

: 346690-28-6
4-benzyloxy-benzo[a]phenazine-11-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 97 percent / conc. HCl / ethanol / 4 h / Heating

2: 55 percent / boron tribromide / CH₂Cl₂ / 16 h / 20 °C

3: NaOH / ethanol / 4 h / Heating

With hydrogenchloride; sodium hydroxide; boron tribromide; In ethanol; dichloromethane;
DOI:10.1021/jm010329a

Reference yield:

: 61539-67-1
5-methoxy[1,2]naphthoquinone

: (4-benzyloxy-benzo[a]phenazin-11-yl)-imidazol-1-yl-methanone

Guidance literature:: Multi-step reaction with 4 steps

1: 97 percent / conc. HCl / ethanol / 4 h / Heating

2: 55 percent / boron tribromide / CH₂Cl₂ / 16 h / 20 °C

3: NaOH / ethanol / 4 h / Heating

4: dimethylformamide / 4 h / 20 °C

With hydrogenchloride; sodium hydroxide; boron tribromide; In ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm010329a