1-Propenyl cyclopentane

Base Information

Chemical Name:1-Propenyl cyclopentane
CAS No.:5623-78-9
Molecular Formula:C8H14
Molecular Weight:110.1968
Hs Code.:
DSSTox Substance ID:DTXSID10204794

Synonyms:1-PROPENYL CYCLOPENTANE;Cyclopentane, propylidene;5623-78-9;DTXSID10204794;JCZSETXGLMHOIT-UHFFFAOYSA-N

Suppliers and Price of 1-Propenyl cyclopentane

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
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price

Total 0 raw suppliers

Chemical Property of 1-Propenyl cyclopentane

Chemical Property:

Vapor Pressure:9.26mmHg at 25°C
Boiling Point:136.1°Cat760mmHg
Flash Point:19.5°C
Density:0.9g/cm³
XLogP3:2.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:1
Exact Mass:110.109550447
Heavy Atom Count:8
Complexity:82.2

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC=C1CCCC1

Technology Process of 1-Propenyl cyclopentane

There total 4 articles about 1-Propenyl cyclopentane 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:

: 3524-75-2
allylcyclopentane

: 3074-61-1
1-propylcyclopentene

: 5623-78-9
(E)-prop-1-en-1-ylcyclopentane

Guidance literature:: With chromium corundum; at 250 ℃;

Reference yield:

: 3524-75-2
allylcyclopentane

: 5623-78-9
(E)-prop-1-en-1-ylcyclopentane

Guidance literature:: With C₂₄H₃₅IrNP; sodium t-butanolate; In benzene-d6; at 25 ℃; for 30h; stereoselective reaction; Inert atmosphere; Glovebox; Schlenk technique;
DOI:10.1002/anie.201611007