Triethyl 1-oxobutane-1,2,3-tricarboxylate

Base Information

Chemical Name:Triethyl 1-oxobutane-1,2,3-tricarboxylate
CAS No.:5464-46-0
Molecular Formula:C₁₃H₂₀O₇
Molecular Weight:288.298
Hs Code.:
NSC Number:15854
DSSTox Substance ID:DTXSID50280198

Synonyms:5464-46-0;triethyl 1-oxobutane-1,2,3-tricarboxylate;NSC15854;DTXSID50280198;NSC 15854;NSC-15854

Suppliers and Price of Triethyl 1-oxobutane-1,2,3-tricarboxylate

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 5 raw suppliers

Chemical Property of Triethyl 1-oxobutane-1,2,3-tricarboxylate

Chemical Property:

Vapor Pressure:7.95E-06mmHg at 25°C
Boiling Point:375.1°Cat760mmHg
Flash Point:163.3°C
Density:1.146g/cm³
XLogP3:1.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:11
Exact Mass:288.12090297
Heavy Atom Count:20
Complexity:375

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of Triethyl 1-oxobutane-1,2,3-tricarboxylate

There total 3 articles about Triethyl 1-oxobutane-1,2,3-tricarboxylate 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:

: 95-92-1
oxalic acid diethyl ester

: 5464-46-0
diethyl 3-ethoxycarbonyl-4-methyl-2-oxopentanedioate

Guidance literature:: With sodium ethanolate;

Reference yield:

: 4100-80-5
2-methylsuccinic anhydride

: 5464-46-0
diethyl 3-ethoxycarbonyl-4-methyl-2-oxopentanedioate

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen chloride

2: sodium ethylate

With hydrogenchloride; sodium ethanolate;