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Methyl (3S)-3-aminobutanoate

Base Information
  • Chemical Name:Methyl (3S)-3-aminobutanoate
  • CAS No.:83509-89-1
  • Molecular Formula:C5H11NO2
  • Molecular Weight:117.148
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40429332
  • Nikkaji Number:J953.818F
  • Wikidata:Q76393904
  • Mol file:83509-89-1.mol
Methyl (3S)-3-aminobutanoate

Synonyms:Methyl (3S)-3-aminobutanoate;83509-89-1;(S)-Methyl 3-aminobutanoate;(S)-3-Aminobutyric acid methyl ester;Butanoic acid, 3-amino-, methyl ester, (3S)-;(S)-Methyl3-aminobutanoate;SCHEMBL1144127;DTXSID40429332;SJQZRROQIBFBPS-BYPYZUCNSA-N;METHYL(3S)-3-AMINOBUTANOATE;AKOS026728697;(S)-3-Aminobutanoic acid methyl ester;EN300-137130;N13255

Suppliers and Price of Methyl (3S)-3-aminobutanoate
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 20 raw suppliers
Chemical Property of Methyl (3S)-3-aminobutanoate
Chemical Property:
  • PSA:52.32000 
  • LogP:0.59700 
  • XLogP3:-0.5
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:3
  • Exact Mass:117.078978594
  • Heavy Atom Count:8
  • Complexity:82.5
Purity/Quality:

≥99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(CC(=O)OC)N
  • Isomeric SMILES:C[C@@H](CC(=O)OC)N
Technology Process of Methyl (3S)-3-aminobutanoate

There total 38 articles about Methyl (3S)-3-aminobutanoate 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 thionyl chloride; at 0 - 10 ℃; Reflux;
Guidance literature:
With hydrogen; palladium on activated charcoal; In ethyl acetate; at 50 ℃; for 25h; under 22800 Torr;
Guidance literature:
With palladium 10% on activated carbon; hydrogen; In ethyl acetate; at 20 ℃; for 14h; under 2844.39 Torr;
DOI:10.1002/anie.201914896
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