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Propanoic acid, 2-hydroxy-, octyl ester, (2S)-

Base Information
  • Chemical Name:Propanoic acid, 2-hydroxy-, octyl ester, (2S)-
  • CAS No.:51191-33-4
  • Molecular Formula:C11H22O3
  • Molecular Weight:202.294
  • Hs Code.:
  • European Community (EC) Number:257-041-4
  • DSSTox Substance ID:DTXSID8074364
  • Nikkaji Number:J70.523C
  • Wikidata:Q81977034
  • Mol file:51191-33-4.mol
Propanoic acid, 2-hydroxy-, octyl ester, (2S)-

Synonyms:Octyl (S)-lactate;51191-33-4;octyl lactate;Propanoic acid, 2-hydroxy-, octyl ester, (2S)-;EINECS 257-041-4;Octyl(S)-lactate;(?)-L-Lactic acid octyl ester;DTXSID8074364;2-hydroxy-propionic acid octyl ester

Suppliers and Price of Propanoic acid, 2-hydroxy-, octyl ester, (2S)-
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 6 raw suppliers
Chemical Property of Propanoic acid, 2-hydroxy-, octyl ester, (2S)-
Chemical Property:
  • Vapor Pressure:0.00377mmHg at 25°C 
  • Melting Point:-8 °C 
  • Boiling Point:249°Cat760mmHg 
  • Flash Point:103.2°C 
  • PSA:46.53000 
  • Density:0.956g/cm3 
  • LogP:2.27090 
  • XLogP3:3.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:9
  • Exact Mass:202.15689456
  • Heavy Atom Count:14
  • Complexity:146
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCCCOC(=O)C(C)O
  • Isomeric SMILES:CCCCCCCCOC(=O)[C@H](C)O
Technology Process of Propanoic acid, 2-hydroxy-, octyl ester, (2S)-

There total 1 articles about Propanoic acid, 2-hydroxy-, octyl ester, (2S)- 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:
Guidance literature:
With di-tert-butyl-diazodicarboxylate; triphenylphosphine; In tetrahydrofuran; Inert atmosphere;
DOI:10.1080/15421406.2011.569689
Guidance literature:
With di-tert-butyl-diazodicarboxylate; triphenylphosphine; In tetrahydrofuran; Inert atmosphere;
DOI:10.1080/15421406.2011.569689
upstream raw materials:

octanol

L-Lactic acid

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