2-Amino-N-[2-(3,4-dimethoxyphenyl)ethyl]-4,5-dimethoxybenzamide

Base Information

Chemical Name:2-Amino-N-[2-(3,4-dimethoxyphenyl)ethyl]-4,5-dimethoxybenzamide
CAS No.:125232-08-8
Molecular Formula:C₁₉H₂₄N₂O₅
Molecular Weight:360.41
Hs Code.:
DSSTox Substance ID:DTXSID301173906

Synonyms:DTXSID301173906;2-Amino-N-[2-(3,4-dimethoxyphenyl)ethyl]-4,5-dimethoxybenzamide;125232-08-8

Suppliers and Price of 2-Amino-N-[2-(3,4-dimethoxyphenyl)ethyl]-4,5-dimethoxybenzamide

Supply Marketing:

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

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Chemical Property of 2-Amino-N-[2-(3,4-dimethoxyphenyl)ethyl]-4,5-dimethoxybenzamide

Chemical Property:

XLogP3:2.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:8
Exact Mass:360.16852187
Heavy Atom Count:26
Complexity:436

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=C(C=C(C=C1)CCNC(=O)C2=CC(=C(C=C2N)OC)OC)OC

Technology Process of 2-Amino-N-[2-(3,4-dimethoxyphenyl)ethyl]-4,5-dimethoxybenzamide

There total 8 articles about 2-Amino-N-[2-(3,4-dimethoxyphenyl)ethyl]-4,5-dimethoxybenzamide 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: 22.0%

: 125231-99-4
N-[2-(3,4-Dimethoxy-phenyl)-ethyl]-4,5-dimethoxy-2-nitro-benzamide

: 125232-08-8
2-Amino-N-[2-(3,4-dimethoxy-phenyl)-ethyl]-4,5-dimethoxy-benzamide

Guidance literature:: With ammonium hydroxide; iron(II) sulfate; In water; Heating;

Reference yield:

: 121-33-5,8014-42-4
vanillin

: 125232-08-8
2-Amino-N-[2-(3,4-dimethoxy-phenyl)-ethyl]-4,5-dimethoxy-benzamide

Guidance literature:: Multi-step reaction with 5 steps

3: LAH

4: 47 percent / benzene / Ambient temperature

5: 22 percent / FeSO₄*7H₂O, NH₄OH / H₂O / Heating

With ammonium hydroxide; lithium aluminium tetrahydride; iron(II) sulfate; In water; benzene;

Reference yield:

: 120-14-9
3,4-dimethoxy-benzaldehyde

: 125232-08-8
2-Amino-N-[2-(3,4-dimethoxy-phenyl)-ethyl]-4,5-dimethoxy-benzamide

Guidance literature:: Multi-step reaction with 4 steps

2: LAH

3: 47 percent / benzene / Ambient temperature

4: 22 percent / FeSO₄*7H₂O, NH₄OH / H₂O / Heating

With ammonium hydroxide; lithium aluminium tetrahydride; iron(II) sulfate; In water; benzene;