Buta-1,3-diene-1,4-dione

Base Information

Chemical Name:Buta-1,3-diene-1,4-dione
CAS No.:2829-38-1
Molecular Formula:C4H2O2
Molecular Weight:82.0587
Hs Code.:
DSSTox Substance ID:DTXSID30572947
Nikkaji Number:J598.089E

Synonyms:2829-38-1;Buta-1,3-diene-1,4-dione;DTXSID30572947

Suppliers and Price of Buta-1,3-diene-1,4-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 2 raw suppliers

Chemical Property of Buta-1,3-diene-1,4-dione

Chemical Property:

XLogP3:1.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:82.005479302
Heavy Atom Count:6
Complexity:97.5

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C(=C=O)C=C=O

Technology Process of Buta-1,3-diene-1,4-dione

There total 1 articles about Buta-1,3-diene-1,4-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:

: 40301-85-7
1,4-bis-diazo-butane-2,3-dione

: 2961-80-0
2-cyclopropene-1-one

: 2829-38-1
1,4-dioxo-1,3-butadiene

: 4-Diazo-but-1-ene-1,3-dione

: 74-86-2,25067-58-7
acetylene

Guidance literature:: With argon; In gaseous matrix; at -263.2 ℃; for 13h; Product distribution; Irradiation; in dependence on λ, time;

Reference yield:

: 2829-38-1
1,4-dioxo-1,3-butadiene

: 98664-89-2,98718-37-7
(6aRS,9aSR,9SR)-ethyl 6,6a,7,8,9,9a-hexahydro-7,7-dimethylisoindolo[4,5,6-cd]indole-9-carboxylate

: 83136-88-3
(+/-)-α-cyclopiazonic acid

Guidance literature:: With potassium tert-butylate; Yield given. Multistep reaction; 1.) CH₂Cl₂, reflux, 2 h, 2.) THF, EtOH, from 0 deg C to RT, 15 h;