N-Ethyl-2-pyrrolidylmethyl phenylcyclopentylglycolate

Base Information

• Chemical Name: N-Ethyl-2-pyrrolidylmethyl phenylcyclopentylglycolate
• CAS No.: 7199-05-5
• Molecular Formula: C20H29NO3
• UNII: KJ5DSO5R52
• Nikkaji Number: J395.116B
• Mol file: 7199-05-5.mol

Synonyms:Pyrrolidyl isomer of ditran;KJ5DSO5R52;UNII-KJ5DSO5R52;N-Ethyl-2-pyrrolidylmethyl phenylcyclopentylglycolate;7199-05-5;Mandelic acid, alpha-cyclopentyl-, (1-ethyl-2-pyrrolidinyl)methyl ester;Benzeneacetic acid, alpha-cyclopentyl-alpha-hydroxy-, (1-ethyl-2-pyrrolidinyl)methyl ester;Cyclopentylphenylglycolic acid 1-ethyl-2-pyrrolidinylmethyl ester;MANDELIC ACID, .ALPHA.-CYCLOPENTYL-, (1-ETHYL-2-PYRROLIDINYL)METHYL ESTER;BENZENEACETIC ACID, .ALPHA.-CYCLOPENTYL-.ALPHA.-HYDROXY-, (1-ETHYL-2-PYRROLIDINYL)METHYL ESTER

Chemical Property of N-Ethyl-2-pyrrolidylmethyl phenylcyclopentylglycolate

Chemical Property:

• XLogP3: 3.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 7
• Exact Mass: 331.21474379
• Heavy Atom Count: 24
• Complexity: 415

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCN1CCCC1COC(=O)C(C2CCCC2)(C3=CC=CC=C3)O

Technology Process of N-Ethyl-2-pyrrolidylmethyl phenylcyclopentylglycolate

There total 1 articles about N-Ethyl-2-pyrrolidylmethyl 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:

→ -phenylcyclopentylglykolat (7199-05-5)

Guidance literature:

aus N-Aethyl-2-pyrrolidylmethanol, Methyl-phenylcyclopentylglykolat, NaOMe in Heptan (4 h sd.);

DOI:10.1021/jo01068a108