2-Methyl-N-[(E)-1-phenylethylidene]-1-propanamine

Base Information

Chemical Name:2-Methyl-N-[(E)-1-phenylethylidene]-1-propanamine
CAS No.:19340-97-7
Molecular Formula:C12H17 N
Molecular Weight:175.27
Hs Code.:2921499090
Mol file:19340-97-7.mol

Synonyms:Propylamine,2-methyl-N-(a-methylbenzylidene)-(8CI); Acetophenone N-isobutylimine

Suppliers and Price of 2-Methyl-N-[(E)-1-phenylethylidene]-1-propanamine

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 2-Methyl-N-[(E)-1-phenylethylidene]-1-propanamine

Chemical Property:

PSA：12.36000
LogP:3.15160

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 2-Methyl-N-[(E)-1-phenylethylidene]-1-propanamine

There total 2 articles about 2-Methyl-N-[(E)-1-phenylethylidene]-1-propanamine 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: 62.0%

: 72-18-4,25609-85-2,7004-03-7,921-10-8
L-valine

: 98-86-2
acetophenone

: 19340-97-7
N-isobutyl-1-phenylethan-1-imine

Guidance literature:: at 135 ℃; for 96h;
DOI:10.1039/c7gc02167d

Reference yield:

: α-Isobutylamino-isobutyronitril

: 98-86-2
acetophenone

: 19340-97-7
N-isobutyl-1-phenylethan-1-imine

Guidance literature:: DOI:10.1016/S0040-4020(01)98664-8

Reference yield: 85.0%

: 19340-97-7
N-isobutyl-1-phenylethan-1-imine

: C₁₂H₁₉N

Guidance literature:: With trichlorosilane; C₁₆H₂₄F₂N₂O₂S; In toluene; at -40 ℃; for 48h; enantioselective reaction; Inert atmosphere;
DOI:10.1039/c4ob01257g