Methyl 2-(2,5-dioxooxolan-3-yl)acetate

Base Information

Chemical Name:Methyl 2-(2,5-dioxooxolan-3-yl)acetate
CAS No.:88067-07-6
Molecular Formula:C₇H₈O₅
Molecular Weight:172.138
Hs Code.:
European Community (EC) Number:833-297-8

Synonyms:methyl 2-(2,5-dioxooxolan-3-yl)acetate;88067-07-6;methyl (2,5-dioxotetrahydrofuran-3-yl)acetate;AKOS006278254;methyl2-(2,5-dioxooxolan-3-yl)acetate;EN300-246711;AI-942/25034418

Suppliers and Price of Methyl 2-(2,5-dioxooxolan-3-yl)acetate

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

American Custom Chemicals Corporation
METHYL (2,5-DIOXOTETRAHYDROFURAN-3-YL)ACETATE 95.00%
5MG
$ 497.08

Total 4 raw suppliers

Chemical Property of Methyl 2-(2,5-dioxooxolan-3-yl)acetate

Chemical Property:

XLogP3:-0.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:172.03717335
Heavy Atom Count:12
Complexity:232

Purity/Quality:

97% ^*data from raw suppliers

METHYL (2,5-DIOXOTETRAHYDROFURAN-3-YL)ACETATE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC(=O)CC1CC(=O)OC1=O

Technology Process of Methyl 2-(2,5-dioxooxolan-3-yl)acetate

There total 2 articles about Methyl 2-(2,5-dioxooxolan-3-yl)acetate 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:

: 99-14-9
tricarallylic acid

: 88067-07-6
propane-1,2,3-tricarboxylic acid-1,2-anhydride-3-methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: acetic acid anhydride / 45 °C

2: diethyl ether; acetone

With diethyl ether; acetic anhydride; acetone;