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(S)-methyl 2-methylcarbonyloxypropanoate

Base Information
  • Chemical Name:(S)-methyl 2-methylcarbonyloxypropanoate
  • CAS No.:14031-88-0
  • Molecular Formula:C6H10O4
  • Molecular Weight:146.143
  • Hs Code.:
  • DSSTox Substance ID:DTXSID70453327
  • Nikkaji Number:J1.153.871A
  • Wikidata:Q82274448
  • Mol file:14031-88-0.mol
(S)-methyl 2-methylcarbonyloxypropanoate

Synonyms:Methyl (S)-2-acetoxypropanoate;14031-88-0;(S)-methyl 2-methylcarbonyloxypropanoate;methyl (2S)-2-acetyloxypropanoate;Propanoic acid, 2-(acetyloxy)-, methyl ester, (2S)-;SCHEMBL5864497;DTXSID70453327;QTFFGYLLUHQSAS-BYPYZUCNSA-N;methyl (2S)-2-(acetyloxy)propanoate;(S)-2-Acetoxypropanoic acid methyl ester;BS-49011;CS-0161605;E75617

Suppliers and Price of (S)-methyl 2-methylcarbonyloxypropanoate
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 3 raw suppliers
Chemical Property of (S)-methyl 2-methylcarbonyloxypropanoate
Chemical Property:
  • XLogP3:0.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:4
  • Exact Mass:146.05790880
  • Heavy Atom Count:10
  • Complexity:141
Purity/Quality:

99.90% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C(=O)OC)OC(=O)C
  • Isomeric SMILES:C[C@@H](C(=O)OC)OC(=O)C
Technology Process of (S)-methyl 2-methylcarbonyloxypropanoate

There total 11 articles about (S)-methyl 2-methylcarbonyloxypropanoate 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 phenylacetone monooxygenase from Thermobifida fusca; glucose-6-phosphate dehydrogenase; glucose-6-phosphate; NADPH; In dimethyl sulfoxide; at 30 ℃; for 24h; pH=9; optical yield given as %ee; enantioselective reaction; aq. buffer; Enzymatic reaction;
DOI:10.1002/anie.201103348
Guidance literature:
With sodium periodate; ruthenium tetroxide; Yield given. Multistep reaction; 1.) CCl4, MeCN, H2O, 44 h, room temp., 2.) ether;
DOI:10.1021/jo00162a009
Guidance literature:
With rhodium(I)-bis(1,5-cyclooctadiene) tetrafluoroborate; diphosphines type FERRIPHOS ligand; hydrogen; In acetone; for 12h; under 750.06 Torr; Yield given; Yields of byproduct given. Title compound not separated from byproducts; Ambient temperature;
DOI:10.1016/S0957-4166(99)00182-2
upstream raw materials:

(S)-Methyl lactate

acetyl chloride

diazomethane

L-Lactic acid

Downstream raw materials:

(S)-Methyl lactate

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