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(2S)-2-Ethylhexyl acetate

Base Information
  • Chemical Name:(2S)-2-Ethylhexyl acetate
  • CAS No.:50373-28-9
  • Molecular Formula:C10H20O2
  • Molecular Weight:172.268
  • Hs Code.:
  • European Community (EC) Number:256-556-1
  • Nikkaji Number:J1.281.051B
  • Wikidata:Q27160444
  • Mol file:50373-28-9.mol
(2S)-2-Ethylhexyl acetate

Synonyms:(2S)-2-Ethylhexyl acetate;(+)-2-Ethylhexyl acetate;EINECS 256-556-1;50373-28-9;[(2S)-2-ethylhexyl] acetate;(2S)-2-Ethylhexyl acetic acid;acetic acid 2-ethyl-hexyl ester;SCHEMBL14625765;CHEBI:88553;Acetic acid (S)-2-ethylhexyl ester;Q27160444

Suppliers and Price of (2S)-2-Ethylhexyl acetate
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 4 raw suppliers
Chemical Property of (2S)-2-Ethylhexyl acetate
Chemical Property:
  • Boiling Point:195.7°Cat760mmHg 
  • Flash Point:71.4°C 
  • Density:0.872g/cm3 
  • XLogP3:3.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:7
  • Exact Mass:172.146329876
  • Heavy Atom Count:12
  • Complexity:121
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCC(CC)COC(=O)C
  • Isomeric SMILES:CCCC[C@H](CC)COC(=O)C
Technology Process of (2S)-2-Ethylhexyl acetate

There total 2 articles about (2S)-2-Ethylhexyl acetate 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 lipase from Pseudomonas fluorescens; In dichloromethane; at 30 ℃; for 24h;
Guidance literature:
With lipase from Pseudomonas fluorescens; In dichloromethane; at 0 ℃; for 48h;
Guidance literature:
Multi-step reaction with 2 steps
1: 90 percent / KOH / H2O; ethanol / 20 °C
2: 79 percent / APTS; molecular sieves 4 Angstroem / toluene / 48 h / Heating
With potassium hydroxide; 4 A molecular sieve; 8-aminopyrene-1,3,6-trisulfonic acid, trisodium salt; In ethanol; water; toluene; 1: Hydrolysis / 2: Esterification;
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