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(2S)-2-Hydroxyoctanoic acid

Base Information
  • Chemical Name:(2S)-2-Hydroxyoctanoic acid
  • CAS No.:70267-27-5
  • Molecular Formula:C8H16O3
  • Molecular Weight:160.213
  • Hs Code.:
  • DSSTox Substance ID:DTXSID501313130
  • Nikkaji Number:J1.137.094B
  • Wikidata:Q27097142
  • Metabolomics Workbench ID:151060
(2S)-2-Hydroxyoctanoic acid

Synonyms:(2S)-2-HYDROXYOCTANOIC ACID;(s)-2-hydroxyoctanoic acid;70267-27-5;HOC;S-2-Hydroxyoctanoic acid;(s)-2-hydroxy octanoic acid;SCHEMBL193518;DTXSID501313130;DB07907;Q27097142

Suppliers and Price of (2S)-2-Hydroxyoctanoic acid
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
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Total 0 raw suppliers
Chemical Property of (2S)-2-Hydroxyoctanoic acid
Chemical Property:
  • XLogP3:2
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:6
  • Exact Mass:160.109944368
  • Heavy Atom Count:11
  • Complexity:112
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCC(C(=O)O)O
  • Isomeric SMILES:CCCCCC[C@@H](C(=O)O)O
Technology Process of (2S)-2-Hydroxyoctanoic acid

There total 2 articles about (2S)-2-Hydroxyoctanoic acid 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 (S)-α-hydroxy acid oxidase from Aerococcus viridans; P450 from Clostridium acetobutylicum; dihydrogen peroxide; Flavin mononucleotide; In aq. phosphate buffer; ethanol; at 20 ℃; for 22h; pH=7.4; Reagent/catalyst; enantioselective reaction; Sealed tube; Enzymatic reaction;
DOI:10.1002/anie.201710227
Guidance literature:
With D-lactate oxidase from Gluconobacter oxydans 621H; oxygen; catalase; In aq. buffer; at 30 ℃; for 24h; pH=7.4; Reagent/catalyst; enantioselective reaction; Resolution of racemate; Enzymatic reaction;
DOI:10.1002/cctc.201600536
Guidance literature:
(S)-2-hydroxyoctanoic acid; With NADH; NAD; at 30 ℃; pH=7; aq. potassium phosphate buffer; Inert atmosphere; Enzymatic reaction;
With hydrogenchloride; In water; aq. potassium phosphate buffer;
DOI:10.1016/j.tet.2009.06.051
upstream raw materials:

2-hydroxy-octanoic acid

Octanoic acid

Downstream raw materials:

2-hydroxy-octanoic acid

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