p-Decyloxybenzylidene p-butylaniline

Base Information

Chemical Name:p-Decyloxybenzylidene p-butylaniline
CAS No.:51749-29-2
Molecular Formula:C₂₇H₃₉NO
Molecular Weight:393.613
Hs Code.:2925290090
Mol file:51749-29-2.mol

Synonyms:p-Decyloxybenzylidene p-butylaniline;51749-29-2;p-Decyloxybenzylidene-p-butylaniline;N-(4-butylphenyl)-1-(4-decoxyphenyl)methanimine;4-Butyl-N-((E)-[4-(decyloxy)phenyl]methylidene)aniline;SCHEMBL12416631;MSABKRNOGDWYAE-WEMUOSSPSA-N;MFCD00043648;AKOS032953558;FT-0675984;(E)-4-butyl-N-(4-(decyloxy)benzylidene)aniline;4-Butyl-N-((E)-[4-(decyloxy)phenyl]methylidene)aniline #

Suppliers and Price of p-Decyloxybenzylidene p-butylaniline

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

Matrix Scientific
p-Decyloxybenzylidene p-butylaniline
5g
$ 324.00

Matrix Scientific
p-Decyloxybenzylidene p-butylaniline
1g
$ 82.00

American Custom Chemicals Corporation
PARA-DECYLOXYBENZYLIDENE PARA-BUTYLANILINE 95.00%
1G
$ 660.95

Total 7 raw suppliers

Chemical Property of p-Decyloxybenzylidene p-butylaniline

Chemical Property:

Vapor Pressure:2.75E-10mmHg at 25°C
Refractive Index:1.512
Boiling Point:517.1 °C at 760 mmHg
PKA:4.25±0.50(Predicted)
Flash Point:213.1 °C
PSA：21.59000
Density:0.93 g/cm³
LogP:8.29930
XLogP3:9.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:15
Exact Mass:393.303164868
Heavy Atom Count:29
Complexity:391

Purity/Quality:

98%min ^*data from raw suppliers

p-Decyloxybenzylidene p-butylaniline ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCCCOC1=CC=C(C=C1)C=NC2=CC=C(C=C2)CCCC

Technology Process of p-Decyloxybenzylidene p-butylaniline

There total 2 articles about p-Decyloxybenzylidene p-butylaniline 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: