3-Propylcyclopentene

Base Information

Chemical Name:3-Propylcyclopentene
CAS No.:34067-75-9
Molecular Formula:C8H14
Molecular Weight:110.1968
Hs Code.:2902199090
DSSTox Substance ID:DTXSID80955625
Nikkaji Number:J113.380B
Mol file:34067-75-9.mol

Synonyms:3-PROPYLCYCLOPENTENE;Cyclopentene, 3-propyl-;34067-75-9;3-Propyl-1-cyclopentene;3-PROPYLCYCLOPENT-1-ENE;3-Propylcyclopentene-1;DTXSID80955625;AKOS006276338

Suppliers and Price of 3-Propylcyclopentene

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 1 raw suppliers

Chemical Property of 3-Propylcyclopentene

Chemical Property:

Vapor Pressure:12.9mmHg at 25°C
Refractive Index:1.4324 (estimate)
Boiling Point:128.6°Cat760mmHg
Flash Point:11.3°C
PSA：0.00000
Density:0.809g/cm³
LogP:2.75270
XLogP3:3.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:2
Exact Mass:110.109550447
Heavy Atom Count:8
Complexity:82

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCC1CCC=C1

Technology Process of 3-Propylcyclopentene

There total 2 articles about 3-Propylcyclopentene 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: 42.0%

: 106-94-5
propyl bromide

: 96-40-2
2-cyclopenten-1-yl chloride

: 34067-75-9
1-propyl-2-cyclopentene

Guidance literature:: propyl bromide; With magnesium; In diethyl ether; for 0.5h; Heating;

2-cyclopenten-1-yl chloride; In diethyl ether; at 20 ℃; for 2h; Further stages.;
DOI:10.1021/ja0121538