3-(2-Aminophenyl)propanamide

Base Information

Chemical Name:3-(2-Aminophenyl)propanamide
CAS No.:1664-61-5
Molecular Formula:C₉H₁₂N₂O
Molecular Weight:164.207
Hs Code.:
European Community (EC) Number:963-873-5
DSSTox Substance ID:DTXSID501312651

Synonyms:3-(2-aminophenyl)propanamide;1664-61-5;2-Aminobenzenepropanamide;2-(2-Carbamoylethyl)aniline;SCHEMBL250283;OPESWHVXZZKOFO-UHFFFAOYSA-N;DTXSID501312651;AKOS009448097;CS-0246014;EN300-315224;G39880;Z414316848

Suppliers and Price of 3-(2-Aminophenyl)propanamide

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 3-(2-Aminophenyl)propanamide

Chemical Property:

XLogP3:0.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:164.094963011
Heavy Atom Count:12
Complexity:159

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C(=C1)CCC(=O)N)N

Technology Process of 3-(2-Aminophenyl)propanamide

There total 1 articles about 3-(2-Aminophenyl)propanamide 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:

: 1664-61-5
dihydrocinnamamide

Guidance literature:: 3-(2-Nitro-phenyl)-propionamid , Hydrierung an Raney-Ni/A.;

Reference yield:

: 24686-78-0
1-Benzoyl-4-piperidone

: 1664-61-5
dihydrocinnamamide

: 160587-22-4
N-(1-benzoyl-4-piperidinyl)-2-(2-carbamoylethyl)aniline

Guidance literature:: With acetic acid; PtO₂; In ethanol;

Reference yield:

: 1664-61-5
dihydrocinnamamide

: 1-[1-(2-Hydroxy-benzoyl)-piperidin-4-yl]-3,4-dihydro-1H-quinolin-2-one

Guidance literature:: Multi-step reaction with 5 steps

1: H₂, acetic acid / PtO₂ / ethanol

2: 5percent aq. HCl

3: H₂ / Pd/C

4: triethylamine / CH₂Cl₂ / Ambient temperature

5: K₂CO₃ / methanol / Ambient temperature

With hydrogenchloride; hydrogen; potassium carbonate; acetic acid; triethylamine; platinum(IV) oxide; palladium on activated charcoal; In methanol; ethanol; dichloromethane;
DOI:10.1021/jm00066a010