2-Amino-N-propylbenzeneacetamide

Base Information

Chemical Name:2-Amino-N-propylbenzeneacetamide
CAS No.:4103-62-2
Molecular Formula:C₁₁H₁₆N₂O
Molecular Weight:192.261
Hs Code.:
DSSTox Substance ID:DTXSID601303120
Nikkaji Number:J782.350I

Synonyms:2-Amino-N-propylbenzeneacetamide;4103-62-2;DTXSID601303120;AKOS000132934

Suppliers and Price of 2-Amino-N-propylbenzeneacetamide

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-propylbenzeneacetamide

Chemical Property:

XLogP3:1.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:192.126263138
Heavy Atom Count:14
Complexity:182

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCNC(=O)CC1=CC=CC=C1N

Technology Process of 2-Amino-N-propylbenzeneacetamide

There total 2 articles about 2-Amino-N-propylbenzeneacetamide 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: 93.0%

: 186966-01-8
N-propyl-(o-nitrophenyl)acetamide

: 4103-62-2
N-n-propyl-(2-aminophenyl)acetamide

Guidance literature:: With iron; ammonium chloride; In isopropyl alcohol; for 1h; Heating;
DOI:10.3987/COM-96-7614

Reference yield:

: 3740-52-1
2-(2-nitrophenyl)acetic acid

: 4103-62-2
N-n-propyl-(2-aminophenyl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / N,N'-carbodiimidazole / ethyl acetate / rt, 2 h then 20 deg C, 1 h

2: 93 percent / Fe, aq. NH₄Cl / propan-2-ol / 1 h / Heating

With iron; ammonium chloride; 1,1'-carbonyldiimidazole; In ethyl acetate; isopropyl alcohol;
DOI:10.3987/COM-96-7614