2-(4-Phenylpiperidin-1-yl)ethanol

Base Information

• Chemical Name: 2-(4-Phenylpiperidin-1-yl)ethanol
• CAS No.: 56953-33-4
• Molecular Formula: C13H19NO
• Molecular Weight: 205.3
• NSC Number: 100212
• DSSTox Substance ID: DTXSID40295195
• Nikkaji Number: J665.249B
• Wikidata: Q82034979
• ChEMBL ID: CHEMBL20399

Synonyms:2-(4-phenylpiperidin-1-yl)ethanol;56953-33-4;CHEMBL20399;NSC100212;NCIOpen2_006638;4-phenyl-1-piperidineethanol;SCHEMBL7281715;DTXSID40295195;MCZUBQLMYYFSGO-UHFFFAOYSA-N;beta-(4-phenyl-piperidino)-ethanol;BDBM50018143;AKOS006342707;2-(4-Phenyl-piperidin-1-yl)-ethanol;NSC-100212;2-(4-PHENYLPIPERIDIN-1-YL)ETHANOL 95%;A1-51505

Chemical Property of 2-(4-Phenylpiperidin-1-yl)ethanol

Chemical Property:

• Vapor Pressure: 4.22E-05mmHg at 25°C
• Boiling Point: 337°C at 760 mmHg
• Flash Point: 162.4°C
• Density: 1.043g/cm³
• XLogP3: 1.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 205.146664230
• Heavy Atom Count: 15
• Complexity: 169

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CN(CCC1C2=CC=CC=C2)CCO

Technology Process of 2-(4-Phenylpiperidin-1-yl)ethanol

There total 3 articles about 2-(4-Phenylpiperidin-1-yl)ethanol 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: 68.0%

oxirane (75-21-8,99932-75-9) + 4-phenylpiperidine (771-99-3) → N-(β-idrossietil)-4-fenilpiperidina (56953-33-4)

Guidance literature:

In n-heptane; at 90 ℃; for 7h;

DOI:10.1021/jm00126a013

Reference yield: 63.0%

4-phenylpiperidine (771-99-3) + 2-bromoethanol (540-51-2) → N-(β-idrossietil)-4-fenilpiperidina (56953-33-4)

Guidance literature:

With potassium carbonate; In acetonitrile; for 4h; Heating;

DOI:10.1021/jm00039a008

Reference yield: 55.0%

4-fenilpiperidina bromidrato + 2-bromoethanol (540-51-2) → N-(β-idrossietil)-4-fenilpiperidina (56953-33-4)

Guidance literature:

upstream raw materials:

oxirane

4-phenylpiperidine

2-bromoethanol

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