4-phenyl-N-[(E)-(2,3,4-trimethoxyphenyl)methylidene]piperazin-1-amine

Base Information

Chemical Name:4-phenyl-N-[(E)-(2,3,4-trimethoxyphenyl)methylidene]piperazin-1-amine
CAS No.:5896-75-3
Molecular Formula:C20H25N3O3
Molecular Weight:355.4308
Hs Code.:
DSSTox Substance ID:DTXSID40417214

Synonyms:5896-75-3;4-phenyl-N-[(E)-(2,3,4-trimethoxyphenyl)methylidene]piperazin-1-amine;307347-58-6;ST50063543;DTXSID40417214;(Z)-N-(4-Phenylpiperazin-1-yl)-1-(2,3,4-trimethoxyphenyl)methanimine;AKOS001634207;BIM-0036258.P001;4-phenyl-N-[(1Z)-(2,3,4-trimethoxyphenyl)methylene]piperazin-1-amine

Suppliers and Price of 4-phenyl-N-[(E)-(2,3,4-trimethoxyphenyl)methylidene]piperazin-1-amine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 4-phenyl-N-[(E)-(2,3,4-trimethoxyphenyl)methylidene]piperazin-1-amine

Chemical Property:

Vapor Pressure:2.08E-11mmHg at 25°C
Boiling Point:532.2°Cat760mmHg
Flash Point:275.7°C
Density:1.13g/cm³
XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:6
Exact Mass:355.18959167
Heavy Atom Count:26
Complexity:434

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C(=C(C=C1)C=NN2CCN(CC2)C3=CC=CC=C3)OC)OC
Isomeric SMILES:COC1=C(C(=C(C=C1)/C=N\N2CCN(CC2)C3=CC=CC=C3)OC)OC

Technology Process of 4-phenyl-N-[(E)-(2,3,4-trimethoxyphenyl)methylidene]piperazin-1-amine

There total 5 articles about 4-phenyl-N-[(E)-(2,3,4-trimethoxyphenyl)methylidene]piperazin-1-amine 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:

: 2973-19-5
2-hydroxy-5-nitrobenzyl chloride

: 5896-75-3
2-(5-Acetamino-2-methoxy-phenylsulfonylmethyl)-4-nitro-1-octyloxy-benzol

Guidance literature:: Multi-step reaction with 2 steps

1: NaI

2: aq. KOH

With potassium hydroxide; sodium iodide;
DOI:10.1039/j39660000873

Reference yield:

: 5896-95-7
5-Acetamino-2-methoxy-benzolsulfinsaeure

: 5896-75-3
2-(5-Acetamino-2-methoxy-phenylsulfonylmethyl)-4-nitro-1-octyloxy-benzol

Guidance literature:: Multi-step reaction with 2 steps

1: NaI

2: aq. KOH

With potassium hydroxide; sodium iodide;
DOI:10.1039/j39660000873

Reference yield:

: 5804-73-9
5-acetamido-2-methoxybenzene-1-sulfonyl chloride

: 5896-75-3
2-(5-Acetamino-2-methoxy-phenylsulfonylmethyl)-4-nitro-1-octyloxy-benzol

Guidance literature:: Multi-step reaction with 3 steps

1: Na₂SO₃*7H₂O, NaOH

2: NaI

3: aq. KOH

With potassium hydroxide; sodium hydroxide; sodium iodide; sodium sulfite;
DOI:10.1039/j39660000873