(E)-N-Benzyl-1-(2,4,6-trimethoxyphenyl)methanimine

Base Information

Chemical Name:(E)-N-Benzyl-1-(2,4,6-trimethoxyphenyl)methanimine
CAS No.:175349-95-8
Molecular Formula:C17H19NO3
Molecular Weight:285.343
Hs Code.:
DSSTox Substance ID:DTXSID20578978

Synonyms:(E)-N-Benzyl-1-(2,4,6-trimethoxyphenyl)methanimine;175349-95-8;DTXSID20578978;N-Benzyl-2,4,6-trimethoxybenzaldimine

Suppliers and Price of (E)-N-Benzyl-1-(2,4,6-trimethoxyphenyl)methanimine

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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Total 0 raw suppliers

Chemical Property of (E)-N-Benzyl-1-(2,4,6-trimethoxyphenyl)methanimine

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:285.13649347
Heavy Atom Count:21
Complexity:301

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC(=C(C(=C1)OC)C=NCC2=CC=CC=C2)OC

Technology Process of (E)-N-Benzyl-1-(2,4,6-trimethoxyphenyl)methanimine

There total 3 articles about (E)-N-Benzyl-1-(2,4,6-trimethoxyphenyl)methanimine 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: 100.0%

: 830-79-5
2,4,6-trimethoxybenzaldehyde

: 100-46-9
benzylamine

: 175349-95-8
Benzyl-[1-(2,4,6-trimethoxy-phenyl)-meth-(E)-ylidene]-amine

Guidance literature:: In toluene; at 45 ℃; for 3h; Molecular sieve;
DOI:10.1055/s-0029-1217076

Reference yield:

: 1361111-11-6
C₁₆H₁₃⁽²⁾H₂BrN₂

: 175349-95-8
Benzyl-[1-(2,4,6-trimethoxy-phenyl)-meth-(E)-ylidene]-amine

Guidance literature:: Multi-step reaction with 3 steps

1: sulfuric acid / 0 °C / Reflux

2: palladium on activated charcoal; ammonium formate

3: potassium carbonate / methanol / 20 °C

With sulfuric acid; palladium on activated charcoal; ammonium formate; potassium carbonate; In methanol;
DOI:10.1016/j.tetlet.2012.01.004

Reference yield:

: 1361110-35-1
methyl 3-(benzylamino)-2,2-dideutero-3-(4-bromophenyl)propanoate

: 175349-95-8
Benzyl-[1-(2,4,6-trimethoxy-phenyl)-meth-(E)-ylidene]-amine

Guidance literature:: Multi-step reaction with 2 steps

1: palladium on activated charcoal; ammonium formate

2: potassium carbonate / methanol / 20 °C

With palladium on activated charcoal; ammonium formate; potassium carbonate; In methanol;
DOI:10.1016/j.tetlet.2012.01.004