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3-Hydroxybutanamide

Base Information
  • Chemical Name:3-Hydroxybutanamide
  • CAS No.:24311-45-3
  • Molecular Formula:C4H9NO2
  • Molecular Weight:103.121
  • Hs Code.:
  • European Community (EC) Number:869-147-3
  • DSSTox Substance ID:DTXSID20332052
  • Nikkaji Number:J26.751A
  • Wikidata:Q27106814
  • Mol file:24311-45-3.mol
3-Hydroxybutanamide

Synonyms:3-hydroxybutanamide;24311-45-3;Butanamide, 3-hydroxy-;n -(1-hydroxyethyl)acetamide;SCHEMBL115227;CHEBI:5588;DTXSID20332052;AKOS006221172;CS-0435186;F84087;EN300-4257758;Q27106814

Suppliers and Price of 3-Hydroxybutanamide
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 5 raw suppliers
Chemical Property of 3-Hydroxybutanamide
Chemical Property:
  • PSA:64.31000 
  • LogP:0.39230 
  • XLogP3:-1.2
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:103.063328530
  • Heavy Atom Count:7
  • Complexity:72.1
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)N)O
Technology Process of 3-Hydroxybutanamide

There total 1 articles about 3-Hydroxybutanamide 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 iodosylbenzene; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1002/ejoc.201101784
Guidance literature:
With Triethoxysilane; o-Ph2P(C6H4)Si(Me)2Fe(H)(PMe3)3; In tetrahydrofuran; at 60 ℃; for 24h; Schlenk technique;
DOI:10.1039/c8dt00289d
upstream raw materials:

3-hydroxybutanenitrile

Downstream raw materials:

5-methyl-1,3-oxazolidin-2-one

3-hydroxybutanenitrile

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