Acetic acid 1,4-dioxo-1,4-dihydronaphthalene-2-yl ester

Base Information Edit

Chemical Name:Acetic acid 1,4-dioxo-1,4-dihydronaphthalene-2-yl ester
CAS No.:1785-65-5
Molecular Formula:C12H8O4
Molecular Weight:216.193
Hs Code.:2915390090
Mol file:1785-65-5.mol

Synonyms:2-(Acetyloxy)-1,4-naphthalenedione;2-Hydroxy-1,4-naphthoquinone acetate;(1,4-dioxonaphthalen-2-yl) acetate;1,4-Naphthoquinone, 2-hydroxy-, acetate;1,4-Naphthalenedione, 2- (acetyloxy)-;2-Acetoxy-1,4-naphthoquinone;1,4-Dioxo-1,4-dihydronaphthalen-2-yl acetate;

Suppliers and Price of Acetic acid 1,4-dioxo-1,4-dihydronaphthalene-2-yl ester

Supply Marketing:Edit

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

TRC
2-Acetoxy-1,4-naphthoquinone
500mg
$ 970.00

Total 7 raw suppliers

Chemical Property of Acetic acid 1,4-dioxo-1,4-dihydronaphthalene-2-yl ester Edit

Chemical Property:

Vapor Pressure:1.66E-05mmHg at 25°C
Refractive Index:1.592
Boiling Point:364.6 °C at 760 mmHg
Flash Point:164 °C
PSA：60.44000
Density:1.34 g/cm³
LogP:1.51260
Solubility.:Dichloromethane; Ethyl Acetate; Methanol

Purity/Quality:

99% ^*data from raw suppliers

2-Acetoxy-1,4-naphthoquinone ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses 2-Acetoxy-1,4-naphthoquinone is an intermediate in the synthesis of Acequinocyl-d25 (A130602). Isotope labelled Acequinocyl is an inhibitor of mitochondrial electron transport in complex III and used to control phytophagous mites. Used in Pesticide detection.

Technology Process of Acetic acid 1,4-dioxo-1,4-dihydronaphthalene-2-yl ester

There total 11 articles about Acetic acid 1,4-dioxo-1,4-dihydronaphthalene-2-yl ester 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: 96.0%

: 83-72-7
2-hydroxynaphtho-1,4-quinone

: 108-24-7
acetic anhydride

: 1785-65-5
2-acetoxy-1,4-naphthoquinone

Guidance literature:: With sulfuric acid; at 20 ℃; for 5h;
DOI:10.1016/j.bmcl.2021.127976

Reference yield: 84.6%

: 83-72-7
2-hydroxynaphtho-1,4-quinone

: 75-36-5
acetyl chloride

: 1785-65-5
2-acetoxy-1,4-naphthoquinone

Guidance literature:: With potassium carbonate; In acetone; at 20 ℃;
DOI:10.1039/b611471g

Reference yield: 21.8%

: 91-20-3,71998-51-1,72931-45-4
naphthalene

: 830-81-9
1-naphthyl acetate

: 5697-00-7
1,4-diacetoxynaphthalene

: 1785-65-5
2-acetoxy-1,4-naphthoquinone

: 130-15-4
[1,4]naphthoquinone

Guidance literature:: With ferrous perchlorate; dihydrogen peroxide; acetic anhydride; acetonitrile; at 30 ℃; for 0.05h; Further byproducts given;