4-Phenyl-1-piperidineacetamide

Base Information

Chemical Name:4-Phenyl-1-piperidineacetamide
CAS No.:84863-82-1
Molecular Formula:C₁₃H₁₈N₂O
Molecular Weight:218.299
Hs Code.:
DSSTox Substance ID:DTXSID701306741

Synonyms:4-Phenyl-1-piperidineacetamide;84863-82-1;2-(4-phenylpiperidin-1-yl)acetamide;SCHEMBL4178029;DTXSID701306741;AKOS034065331;Z287086568

Suppliers and Price of 4-Phenyl-1-piperidineacetamide

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of 4-Phenyl-1-piperidineacetamide

Chemical Property:

XLogP3:1.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:218.141913202
Heavy Atom Count:16
Complexity:228

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CN(CCC1C2=CC=CC=C2)CC(=O)N

Technology Process of 4-Phenyl-1-piperidineacetamide

There total 2 articles about 4-Phenyl-1-piperidineacetamide 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:

: 84864-27-7
ethyl (4-phenyl-1-piperidyl)acetate

: 84863-82-1
2-(4-phenyl-1-piperidyl)acetamide

Guidance literature:: With ammonia; In methanol; for 96h; Yield given; Ambient temperature;
DOI:10.1021/jm00359a015

Reference yield:

: 771-99-3
4-phenylpiperidine

: 84863-82-1
2-(4-phenyl-1-piperidyl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: diisopropylamine / tetrahydrofuran / 72 h / Ambient temperature

2: NH₃ / methanol / 96 h / Ambient temperature

With ammonia; diisopropylamine; In tetrahydrofuran; methanol;
DOI:10.1021/jm00359a015