1-Phenyloctane-1-oneoxime

Base Information

Chemical Name:1-Phenyloctane-1-oneoxime
CAS No.:77611-70-2
Molecular Formula:C14H21NO
Molecular Weight:219.327
Hs Code.:2928000090
Mol file:77611-70-2.mol

Synonyms:1-Octanone,1-phenyl-,oxime;1-phenyl-octan-1-one oxime;phenyl n-heptyl ketone oxime;1-Phenyl-octan-1-on-oxim;

Suppliers and Price of 1-Phenyloctane-1-oneoxime

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-Phenyloctane-1-oneoxime

Chemical Property:

Melting Point:49-50.5 °C
Boiling Point:339.6±11.0 °C(Predicted)
PKA:11.17±0.14(Predicted)
PSA：32.59000
Density:0.95±0.1 g/cm3(Predicted)
LogP:4.22540

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 1-Phenyloctane-1-oneoxime

There total 4 articles about 1-Phenyloctane-1-oneoxime 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:

: 1674-37-9
n-octanophenone

: 77611-70-2
1-Phenyl-octan-1-one oxime

Guidance literature:: With hydroxylamine hydrochloride; sodium acetate; In ethanol; for 1.5h; Yield given; Heating;

Reference yield:

: 1674-37-9
n-octanophenone

: 77611-70-2
phenyl n-heptyl ketone oxime

Guidance literature:: With sodium hydroxide; ethanol; hydroxylamine hydrochloride;

Reference yield:

: 111-64-8
n-octanoic acid chloride

: 77611-70-2
phenyl n-heptyl ketone oxime

Guidance literature:: Multi-step reaction with 2 steps

1: AlCl₃

2: NaOH; diluted alcohol; hydroxylamine hydrochloride

With sodium hydroxide; aluminium trichloride; ethanol; hydroxylamine hydrochloride;