Carbamic acid, [1-(2-propenyl)heptyl]-, phenylmethyl ester

Base Information

Chemical Name:Carbamic acid, [1-(2-propenyl)heptyl]-, phenylmethyl ester
CAS No.:830335-32-5
Molecular Formula:C18H27NO2
Molecular Weight:289.418
Hs Code.:
DSSTox Substance ID:DTXSID30457366
Nikkaji Number:J2.120.467F

Synonyms:830335-32-5;Carbamic acid, [1-(2-propenyl)heptyl]-, phenylmethyl ester;DTXSID30457366;4-(Benzyloxycarbonylamino)-1-decene

Suppliers and Price of Carbamic acid, [1-(2-propenyl)heptyl]-, phenylmethyl ester

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 1 raw suppliers

Chemical Property of Carbamic acid, [1-(2-propenyl)heptyl]-, phenylmethyl ester

Chemical Property:

XLogP3:5.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:11
Exact Mass:289.204179104
Heavy Atom Count:21
Complexity:285

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCC(CC=C)NC(=O)OCC1=CC=CC=C1

Technology Process of Carbamic acid, [1-(2-propenyl)heptyl]-, phenylmethyl ester

There total 2 articles about Carbamic acid, [1-(2-propenyl)heptyl]-, phenylmethyl ester 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: 82.0%

: 111-71-7
heptanal

: 621-84-1
O-benzyl carbamate

: 762-72-1
allyl-trimethyl-silane

: 830335-32-5
(1-hexyl-but-3-enyl)-carbamic acid benzyl ester

Guidance literature:: With copper(II) bis(trifluoromethanesulfonate); In acetonitrile; at 20 ℃; for 8h; Inert atmosphere;
DOI:10.1016/j.tetlet.2009.04.008