Dipentyl cyclohex-4-ene-1,2-dicarboxylate

Base Information

Chemical Name:Dipentyl cyclohex-4-ene-1,2-dicarboxylate
CAS No.:94259-70-8
Molecular Formula:C₁₈H₃₀O₄
Molecular Weight:310.434
Hs Code.:
NSC Number:70999
DSSTox Substance ID:DTXSID90290771
Nikkaji Number:J160.557G

Synonyms:94259-70-8;dipentyl cyclohex-4-ene-1,2-dicarboxylate;NSC70999;SCHEMBL5529348;DTXSID90290771;NSC-70999

Suppliers and Price of Dipentyl cyclohex-4-ene-1,2-dicarboxylate

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 Dipentyl cyclohex-4-ene-1,2-dicarboxylate

Chemical Property:

Vapor Pressure:3.16E-06mmHg at 25°C
Boiling Point:388°Cat760mmHg
Flash Point:182.7°C
Density:1.011g/cm³
XLogP3:4.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:12
Exact Mass:310.21440943
Heavy Atom Count:22
Complexity:328

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCOC(=O)C1CC=CCC1C(=O)OCCCCC

Technology Process of Dipentyl cyclohex-4-ene-1,2-dicarboxylate

There total 3 articles about Dipentyl cyclohex-4-ene-1,2-dicarboxylate 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:

: 71-41-0
pentan-1-ol

: 935-79-5
cis-1,2,3,6-tetrahydrophthalic anhydride

: 94259-70-8
Tetrahydrophthalsaeure-dipentylester

Guidance literature:: With toluene-4-sulfonic acid; at 100 - 140 ℃; Versetzen mit Toluol und erneuten Erhitzen unter Entfernen des gebildeten Wassers;