1-(2-Propenyloxy)heptane

Base Information

Chemical Name:1-(2-Propenyloxy)heptane
CAS No.:16519-24-7
Molecular Formula:C10H20 O
Molecular Weight:156.268
Hs Code.:2909199090
Mol file:16519-24-7.mol

Synonyms:Ether,allyl heptyl (8CI); Heptane, 1-(2-propenyloxy)- (9CI); Allyl heptyl ether;n-Heptyl allyl ether

Suppliers and Price of 1-(2-Propenyloxy)heptane

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 3 raw suppliers

Chemical Property of 1-(2-Propenyloxy)heptane

Chemical Property:

Vapor Pressure:0.758mmHg at 25°C
Boiling Point:190.2°Cat760mmHg
Flash Point:55.1°C
PSA：9.23000
Density:0.801g/cm³
LogP:3.15940

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 1-(2-Propenyloxy)heptane

There total 1 articles about 1-(2-Propenyloxy)heptane 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: 49.0%

: 111-70-6
n-heptan1ol

: 106-95-6
allyl bromide

: 16519-24-7
1-(allyloxy)heptane

Guidance literature:: n-heptan1ol; With sodium hydride; In tetrahydrofuran; at 20 ℃; for 0.5h; Inert atmosphere;

allyl bromide; In tetrahydrofuran; at 20 ℃; Inert atmosphere; Reflux;
DOI:10.1021/acs.orglett.8b02356

Reference yield: 66.0%

: 500-05-0
2H-pyran-2-one-5-carboxylic acid

: 16519-24-7
1-(allyloxy)heptane

: 173265-17-3
4-((heptyloxy)methyl)benzoic acid

Guidance literature:: With palladium 10% on activated carbon; In 1,3,5-trimethyl-benzene; at 200 ℃; regioselective reaction;
DOI:10.1039/c1gc15650k

Reference yield: 51.0%

: 6018-41-3
methyl coumalate

: 16519-24-7
1-(allyloxy)heptane

: 1038734-10-9
methyl 4-(heptyloxymethyl)benzoate

Guidance literature:: With palladium 10% on activated carbon; In 1,3,5-trimethyl-benzene; at 200 ℃; regioselective reaction;
DOI:10.1039/c1gc15650k