N-Phenyl-N-4-piperidinylacetamide

Base Information

• Chemical Name: N-Phenyl-N-4-piperidinylacetamide
• CAS No.: 1607-68-7
• Molecular Formula: C13H18 N2 O
• Molecular Weight: 218.299
• Hs Code.: 2933399090
• European Community (EC) Number: 216-532-3
• NSC Number: 74308
• UNII: C7RP4BKQ2Q
• DSSTox Substance ID: DTXSID40166972
• Nikkaji Number: J195.228E
• Wikidata: Q83036266
• ChEMBL ID: CHEMBL2137667
• Mol file: 1607-68-7.mol

Synonyms:N-Phenyl-N-4-piperidinylacetamide;1607-68-7;n-phenyl-n-(piperidin-4-yl)acetamide;N-phenyl-N-piperidin-4-ylacetamide;Acetyl norfentanyl;MLS002693889;EINECS 216-532-3;NSC-74308;NSC74308;C7RP4BKQ2Q;Acetanilide, N-4-piperidyl-;SCHEMBL6160138;4-(N-Phenylacetamido)piperidine;CHEMBL2137667;DTXSID40166972;CHEBI:189127;HMS3094C11;Piperidine, 4-(N-phenylacetamido)-;N-Phenyl-N-(4-piperidinyl)acetamide;NSC 74308;Acetamide, N-phenyl-N-4-piperidinyl-;AKOS027322359;SMR001559830

 This product is a nationally controlled contraband, and the Lookchem platform doesn't provide relevant sales information.

Chemical Property of N-Phenyl-N-4-piperidinylacetamide

Chemical Property:

• Vapor Pressure: 6.07E-05mmHg at 25°C
• Boiling Point: 345.6°C at 760 mmHg
• Flash Point: 162.8°C
• PSA: 32.34000
• Density: 1.093g/cm³
• LogP: 2.12030
• XLogP3: 1.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 218.141913202
• Heavy Atom Count: 16
• Complexity: 230

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)N(C1CCNCC1)C2=CC=CC=C2

Technology Process of N-Phenyl-N-4-piperidinylacetamide

There total 2 articles about N-Phenyl-N-4-piperidinylacetamide 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:

→ N-phenyl-N-piperidin-4-yl-acetamide (1607-68-7) + Acetanilid (103-84-4)

Guidance literature:

Reference yield:

→ N-phenyl-N-piperidin-4-yl-acetamide (1607-68-7)

Guidance literature:

Reference yield:

N-phenyl-N-piperidin-4-yl-acetamide (1607-68-7) + acetyl chloride (75-36-5) + N-[2-(3,4-dichlorophenyl)-3-formylpropyl]-N-methylbenzamide (160809-30-3,219589-85-2) → N-[4-(4-N'-Acetylanilino-1-piperidinyl)-2-(3,4-dichlorophenyl)butyl]-N-methylbenzamide

Guidance literature:

With sodium cyanoborohydride; In methanol;

Refernces