N-Ethyl-3-piperidyl phenylcyclopentylglycolate

Base Information

• Chemical Name: N-Ethyl-3-piperidyl phenylcyclopentylglycolate
• CAS No.: 467-68-5
• Molecular Formula: C20H30ClNO3
• Molecular Weight: 0
• UNII: B3B8503HM8
• DSSTox Substance ID: DTXSID00963641
• Nikkaji Number: J5.912I
• ChEMBL ID: CHEMBL126644
• Mol file: 467-68-5.mol

Synonyms:467-68-5;N-Ethyl-3-piperidyl phenylcyclopentylglycolate;CHEMBL126644;B3B8503HM8;N-Ethyl-3-piperidyl alpha-phenyl-alpha-cyclopentylglycolate;1-Ethyl-3-piperidyl-alpha-cyclopentyl mandelate;C20H29NO3.ClH;1-ethylpiperidin-3-yl cyclopentyl(hydroxy)phenylacetate;Benzeneacetic acid, .alpha.-cyclopentyl-.alpha.-hydroxy-, 1-ethyl-3-piperidinyl ester, hydrochloride;Oprea1_301019;UNII-B3B8503HM8;DTXSID00963641;BDBM50225737;Mandelic acid, alpha-cyclopentyl-, 1-ethyl-3-piperidyl ester;N-ETHYL-3-PIPERIDYL .ALPHA.-PHENYL-.ALPHA.-CYCLOPENTYLGLYCOLATE;BENZENEACETIC ACID, .ALPHA.-CYCLOPENTYL-.ALPHA.-HYDROXY-, 1-ETHYL-3-PIPERIDINYL ESTER

Chemical Property of N-Ethyl-3-piperidyl phenylcyclopentylglycolate

Chemical Property:

• Vapor Pressure: 2.65E-09mmHg at 25°C
• Boiling Point: 461.2°C at 760 mmHg
• Flash Point: 232.7°C
• PSA: 49.77000
• LogP: 3.02980
• XLogP3: 3.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 6
• Exact Mass: 331.21474379
• Heavy Atom Count: 24
• Complexity: 415

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCN1CCCC(C1)OC(=O)C(C2CCCC2)(C3=CC=CC=C3)O

Technology Process of N-Ethyl-3-piperidyl phenylcyclopentylglycolate

There total 1 articles about N-Ethyl-3-piperidyl phenylcyclopentylglycolate 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:

→ -phenylcyclopentyl-glykolat (467-68-5)

Guidance literature:

aus N-Aethyl-3-hydroxy-piperidin, Methyl-phenylcyclopentylglykolat, NaOMe in Heptan (Rueckfl.); daneben andere Prod.;

DOI:10.1021/jo01068a108