7-oxotridecanedioic Acid

Base Information

Chemical Name:7-oxotridecanedioic Acid
CAS No.:101171-43-1
Molecular Formula:C₁₃H₂₂O₅
Molecular Weight:258.315
Hs Code.:
European Community (EC) Number:600-170-1
DSSTox Substance ID:DTXSID201312876

Synonyms:7-oxotridecanedioic Acid;101171-43-1;SCHEMBL2580866;OETDBDZZHBMHQQ-UHFFFAOYSA-N;DTXSID201312876;7-oxo-tridecane-1,13-dioic acid;AKOS024339725;HY-133952;CS-0135958;6-OXO-1,11-UNDECANEDICARBOXYLIC ACID

Suppliers and Price of 7-oxotridecanedioic Acid

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
7-OXO-TRIDECANEDIOIC ACID 95.00%
5MG
$ 495.41

Total 0 raw suppliers

Chemical Property of 7-oxotridecanedioic Acid

Chemical Property:

Vapor Pressure:5.96E-11mmHg at 25°C
XLogP3:1.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:12
Exact Mass:258.14672380
Heavy Atom Count:18
Complexity:247

Purity/Quality:: 7-OXO-TRIDECANEDIOIC ACID 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

Technology Process of 7-oxotridecanedioic Acid

There total 4 articles about 7-oxotridecanedioic Acid 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:

: 41302-32-3
ethyl 5-iodopentanoate

: 105-50-0
diethyl 1,3-acetonedicarboxylate

: 101171-43-1
7-oxo-tridecane-1,13-dioic acid

Guidance literature:: With sodium ethanolate; Siedend; mehrstuendiges Kochen des entstandenen Tetraaethylesters mit HCl (konz.).;

Reference yield:

: 14660-52-7
ethyl 5-bromovalerate

: 101171-43-1
7-oxo-tridecane-1,13-dioic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium iodide / acetone / 20 °C

2.1: sodium ethanolate / ethanol / Reflux

2.2: Reflux

2.3: Reflux

With sodium ethanolate; sodium iodide; In ethanol; acetone;

Reference yield:

: 670-80-4
4-cyclohexen-1-ylmorpholine

: 101171-43-1
7-oxo-tridecane-1,13-dioic acid

Guidance literature:: With chloroform; triethylamine; Behandeln des Reaktionsgemisches mit Wasser und Natriumhydrogencarbonat; Erhitzen des Reaktionsprodukts mit wss. Natronlauge_.;