Ethyl tetradec-2-enoate

Base Information

Chemical Name:Ethyl tetradec-2-enoate
CAS No.:38112-60-6
Molecular Formula:C16H30O2
Molecular Weight:254.40800
Hs Code.:
DSSTox Substance ID:DTXSID50708120
Mol file:38112-60-6.mol

Synonyms:Ethyl tetradec-2-enoate;ethyl tetradecenate;Ethyl 2-Tetradecenoate;DTXSID50708120;JXDGEQAWGZXILF-UHFFFAOYSA-N

Suppliers and Price of Ethyl tetradec-2-enoate

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

TRC
(E)-EthylTetradec-2-enoate
50g
$ 180.00

TRC
(E)-EthylTetradec-2-enoate
10g
$ 70.00

TRC
(E)-EthylTetradec-2-enoate
5g
$ 50.00

Total 3 raw suppliers

Chemical Property of Ethyl tetradec-2-enoate

Chemical Property:

Boiling Point:115 °C(Press: 2 Torr)
PSA：26.30000
Density:0.878±0.06 g/cm3(Predicted)
LogP:5.02660
XLogP3:6.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:13
Exact Mass:254.224580195
Heavy Atom Count:18
Complexity:209

Purity/Quality:

99% ^*data from raw suppliers

(E)-EthylTetradec-2-enoate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCCCCC=CC(=O)OCC
Uses (E)-Ethyl Tetradec-2-enoate is an intermediate in the synthesis of D-erythro-Sphingosine-1-phosphate-13C2,D2 (S681502), which is a labelled putative lipid second messenger; found to inhibit cellular mobility of melanoma cells at very low concentrations with no toxic effects thereby making it a possible agent for prevention of tumor cell metastasis and inflammatory processes; mobilizes intracellular calcium stores; decreases cellular cAMP; activates phospholipase D; does not inhibitprotein kinase C.

Technology Process of Ethyl tetradec-2-enoate

There total 9 articles about Ethyl tetradec-2-enoate 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: 97.0%